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Parker Quality & Compliance

PQC Reg Watch

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Device type

Laparoscope, General & Plastic Surgery

Product code GCJ · Class II · 21 CFR 876.1500 · Gastroenterology, Urology

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 at https://www.gpo.gov/fdsys/pkg/FR-2017-06-09/pdf/2017-12007.pdf).

FDA classification database

Recent 510(k)s

Recent recalls

No recalls in the archive for GCJ.