Ex Parte YIANNI - Page 4


                 Appeal No.  1999-2816                                                     Page 4                   
                 Application No.  08/064,052                                                                        

                 The examiner finds (Answer, bridging sentence, pages 6-7) that increased                           
                 “lubricity is inherent in the use of the materials disclosed in the prior art.”  In this           
                 regard, we note that while Bird was originally applied4 in a rejection under                       
                 35 U.S.C. § 102(b) during the prosecution of this application, the rejection before                
                 us for review is not based upon anticipation, but is instead one of obviousness                    
                 under 35 U.S.C. § 103.   Therefore, to the extent that the examiner may find                       
                 “increased lubricity” inherent in Bird, we remind the examiner as set forth in In re               
                 Spormann, 363 F.2d 444, 448, 150 USPQ 449, 452 (CCPA 1966) “[t]hat which                           
                 may be inherent is not necessarily known.  Obviousness cannot be predicated                        
                 on what is unknown.”                                                                               
                       Besides failing to mention “lubricity,” Bird differs from the claimed                        
                 invention in not teaching “a single-use disposable device in which a portion of the                
                 surface of the device … is inserted into the body and contacts body tissue….”                      
                 While appellant’s specification does disclose, at page 12, “cuvettes” as “[t]ypical                
                 blood contacting devices,” the limitations set forth in the claims circumscribe a                  
                 subset of the devices listed in the specification.  In our opinion, a person of                    
                 ordinary skill in the art would appreciate that a cuvette would typically not be                   
                 considered a device that would be inserted into the body.  In this regard, we note                 
                 that the examiner has not provided evidence to the contrary.  Instead, the                         
                 examiner finds (Answer, page 5) that “Bird also suggests the use of the                            
                 phosphatidyl choline [sic] material as a biomaterial to be used in a device which                  
                 would be implanted in the body (note, e.g. the suggestion of benefits for grafts in                
                                                                                                                    
                 4 Paper No. 8, mailed June 27, 1994, at page 4, paragraph no. 5.                                   





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