Intromit Hand Access Port for Hand Assisted Laparoscopic Surgery, Model Fp880-150

K990663 is the FDA 510(k) clearance record for INTROMIT HAND ACCESS PORT FOR HAND ASSISTED LAPAROSCOPIC SURGERY, MODEL FP880-150, a class II device, cleared for Medtech , Ltd. on 1999-05-27 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 9 510(k) clearances for Medtech , Ltd., from 1999-05-27 to 2020-05-29. As of 2026-09-10, FDA records show no recalls naming K990663.