LIEBERMAN POLACK DOUBLE CORNEAL FORCEPS

LIEBERMAN POLACK DOUBLE CORNEAL FORCEPS is an FDA 510(k)-cleared medical device (K771003) manufactured by Edward Weck, Inc.. This device is classified under the Ophthalmic specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on June 16, 1977. Regulation: 8.