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FDA 510(k), K052692, SURETEK MEDICAL REPROCESSED ELECTROSURGICAL ELECTRODES
FDA 510(k), K052692, SURETEK MEDICAL REPROCESSED ELECTROSURGICAL ELECTRODES
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510(K) Number: K052692
Device Name: SURETEK MEDICAL REPROCESSED ELECTROSURGICAL ELECTRODES
Manufacturer: MIKE SAMMON
Device Classification Name: Electrosurgical, Cutting & Coagulation Accessories, Laparoscopic & Endoscopic, Reprocessed
Regulation Number: NUJ
Classification Product Code: 09/28/2005
Date Received: 05/10/2006
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: General & Plastic Surgery
Device Name: SURETEK MEDICAL REPROCESSED ELECTROSURGICAL ELECTRODES
Manufacturer: MIKE SAMMON
Device Classification Name: Electrosurgical, Cutting & Coagulation Accessories, Laparoscopic & Endoscopic, Reprocessed
Regulation Number: NUJ
Classification Product Code: 09/28/2005
Date Received: 05/10/2006
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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