
Procter & Gamble Mfg. Co.
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INSTRUMENT PAD is an FDA 510(k)-cleared medical device (K791864) manufactured by Procter & Gamble Mfg. Co.. This device is classified under the General, Plastic Surgery specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on October 16, 1979. Regulation: 8.