
Plastic Injectors, Inc.
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CODE-A-WELL SERIES 1-600, 1-625 is an FDA 510(k)-cleared medical device (K863374) manufactured by Plastic Injectors, Inc.. This device is classified under the Microbiology specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on September 10, 1986. Regulation: 8.

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