Tissuebag, Models: A10 211, A10 212, Tbi 100, Tbi1011, Tbi1021

K092821 is the FDA 510(k) clearance record for TISSUEBAG, MODELS: A10 211, A10 212, TBI 100, TBI1011, TBI1021, a class II device, cleared for Agency For Medical Innovations, Inc. on 2010-02-01 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 5 510(k) clearances for Agency For Medical Innovations, Inc., from 2010-02-01 to 2021-11-10. As of 2026-09-10, FDA records show no recalls naming K092821.