
Keeler Instruments, Inc.
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DONALDSON NATURAL EYEPATCH 'PATIENT PAK' is an FDA 510(k)-cleared medical device (K874411) manufactured by Keeler Instruments, Inc.. This device is classified under the General, Plastic Surgery specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on January 26, 1988. Regulation: 8.