Kodak Pro-Medical Digital Camera System

K973430 is the FDA 510(k) clearance record for KODAK PRO-MEDICAL DIGITAL CAMERA SYSTEM, a class II device, cleared for Eastman Kodak Company on 1998-07-17 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 291 510(k) clearances for Eastman Kodak Company, from 1977-05-26 to 2026-03-11. As of 2026-09-10, FDA records show no recalls naming K973430.