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FDA 510(k), K962587, CONCEPTUS FALLOPIAN TUBE CATHETEIZATION WITH MICROENDOSCOPY SYSTEM
FDA 510(k), K962587, CONCEPTUS FALLOPIAN TUBE CATHETEIZATION WITH MICROENDOSCOPY SYSTEM
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510(K) Number: K962587
Device Name: CONCEPTUS FALLOPIAN TUBE CATHETEIZATION WITH MICROENDOSCOPY SYSTEM
Manufacturer: CONCEPTUS, INC.
Device Classification Name: Falloposcope
Regulation Number: 884.1690
Classification Product Code: MKO
Date Received: 07/01/1996
Decision Date: 01/31/1997
Regulation Medical Specialty: Obstetrics/Gynecology
Device Name: CONCEPTUS FALLOPIAN TUBE CATHETEIZATION WITH MICROENDOSCOPY SYSTEM
Manufacturer: CONCEPTUS, INC.
Device Classification Name: Falloposcope
Regulation Number: 884.1690
Classification Product Code: MKO
Date Received: 07/01/1996
Decision Date: 01/31/1997
Regulation Medical Specialty: Obstetrics/Gynecology
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