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FDA 510(k), K121855, RESPROCESSED SERFAS ENERGY PROBE
FDA 510(k), K121855, RESPROCESSED SERFAS ENERGY PROBE
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510(K) Number: K121855
Device Name: RESPROCESSED SERFAS ENERGY PROBE
Manufacturer: ERIC VARTY
Device Classification Name: Electrosurgical, Cutting & Coagulation Accessories, Laparoscopic & Endoscopic, Reprocessed
Regulation Number: NUJ
Classification Product Code: 06/25/2012
Date Received: 08/16/2012
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: General & Plastic Surgery
Device Name: RESPROCESSED SERFAS ENERGY PROBE
Manufacturer: ERIC VARTY
Device Classification Name: Electrosurgical, Cutting & Coagulation Accessories, Laparoscopic & Endoscopic, Reprocessed
Regulation Number: NUJ
Classification Product Code: 06/25/2012
Date Received: 08/16/2012
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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