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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
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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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks when the FOIA office is operating at regular capacity
NOTE: This document is not currently in our library. Upon purchase, we will request the document from the FDA FOIA office. Learn more about Fast-Track Requests here.
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