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FDA 510(k), K072814, CONVENIENCE KIT FOR SINGLE-INCISION LAPAROSCOPIC SURGERY AND OTHER ADVANCED LAPAROSCOPIC PROCEDURES
FDA 510(k), K072814, CONVENIENCE KIT FOR SINGLE-INCISION LAPAROSCOPIC SURGERY AND OTHER ADVANCED LAPAROSCOPIC PROCEDURES
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510(K) Number: K072814
Device Name: CONVENIENCE KIT FOR SINGLE-INCISION LAPAROSCOPIC SURGERY AND OTHER ADVANCED LAPAROSCOPIC PROCEDURES
Manufacturer: ROBERT ZOTT
Device Classification Name: Kit, Surgical Instrument, Disposable
Regulation Number: KDD
Classification Product Code: 10/01/2007
Date Received: 04/16/2008
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: General & Plastic Surgery
Device Name: CONVENIENCE KIT FOR SINGLE-INCISION LAPAROSCOPIC SURGERY AND OTHER ADVANCED LAPAROSCOPIC PROCEDURES
Manufacturer: ROBERT ZOTT
Device Classification Name: Kit, Surgical Instrument, Disposable
Regulation Number: KDD
Classification Product Code: 10/01/2007
Date Received: 04/16/2008
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: General & Plastic Surgery
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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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