Reusable Laparoscopic Instruments

K930667 is the FDA 510(k) clearance record for REUSABLE LAPAROSCOPIC INSTRUMENTS, a class II device, cleared for Snowden-Pencer on 1994-05-16 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 11 510(k) clearances for Snowden-Pencer, from 1986-06-19 to 2003-04-04. As of 2026-09-10, FDA records show 15 recalls naming K930667.