Intraducer Peritoneal Catheter 6Frx3, 9Frx3 1/2, 10Frx4, 12Frx8

K960883 is the FDA 510(k) clearance record for INTRADUCER PERITONEAL CATHETER 6FRX3, 9FRX3 1/2, 10FRX4, 12FRX8, a class II device, cleared for Taut, Inc. on 1996-03-20 under FDA product code GCJ (Laparoscope, General & Plastic Surgery). FDA's definition for product code GCJ reads: "Validated reprocessing instructions and reprocessing validation data for this device type must be included in a 510(k) submission if the device is reusable and has specific design features (please refer to Table 2 of 82 FR 26807, available...". FDA records list 15 510(k) clearances for Taut, Inc., from 1988-03-08 to 2002-12-13. As of 2026-09-10, FDA records show one recall naming K960883.