
J. Sklar Mfg. Co., Inc.
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TISCHLER CERVICAL BIOPSY PUNCH FORCEPS is an FDA 510(k)-cleared medical device (K842112) manufactured by J. Sklar Mfg. Co., Inc.. This device is classified under the Obstetrics/Gynecology specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on July 2, 1984. Regulation: 8.

Ansell
SKU MSC846624

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SKU VM-1270031