FDA 510(k), K910875, ENDOPATH DISPOSABLE PNEUMOPERITONEUM NEEDLE

FDA 510(k), K910875, ENDOPATH DISPOSABLE PNEUMOPERITONEUM NEEDLE

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510(K) Number: K910875
Device Name: ENDOPATH DISPOSABLE PNEUMOPERITONEUM NEEDLE
Manufacturer: ETHICON, INC.
Device Classification Name: apparatus, pneumoperitoneum, automatic
Regulation Number: 876.1500
Classification Product Code: FDP
Date Received: 03/01/1991
Decision Date: 03/19/1991
Regulation Medical Specialty: Gastroenterology/Urology

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