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FDA 510(k), K943393, CIVCO PROBE BOOT/CORD COVER
FDA 510(k), K943393, CIVCO PROBE BOOT/CORD COVER
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510(K) Number: K943393
Device Name: CIVCO PROBE BOOT/CORD COVER
Manufacturer: J. WILLIAM JONES
Device Classification Name: Drape, Surgical
Regulation Number: KKX
Classification Product Code: 07/14/1994
Date Received: 02/02/1995
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: General Hospital
Device Name: CIVCO PROBE BOOT/CORD COVER
Manufacturer: J. WILLIAM JONES
Device Classification Name: Drape, Surgical
Regulation Number: KKX
Classification Product Code: 07/14/1994
Date Received: 02/02/1995
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: General Hospital
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks
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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