FDA 510(k), K142204, Bioceptive Suction Cervical Retractor

FDA 510(k), K142204, Bioceptive Suction Cervical Retractor

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510(K) Number: K142204
Device Name: Bioceptive Suction Cervical Retractor
Manufacturer: Bioceptive Inc.
Device Classification Name: tenaculum, uterine
Regulation Number: 884.4530
Classification Product Code: HDC
Date Received: 08/11/2014
Decision Date: 12/19/2014
Regulation Medical Specialty: Obstetrics/Gynecology

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