
Pollak (Intl.), Ltd.
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CULSWAB CAT.#978 & 979 is an FDA 510(k)-cleared medical device (K802023) manufactured by Pollak (Intl.), Ltd.. This device is classified under the Microbiology specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on September 8, 1980. Regulation: 8.

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