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FDA 510(k), K122278, BAYLIS MEDICAL COMPANY RADIOFREQUENCY PERFORATION GENERATOR
FDA 510(k), K122278, BAYLIS MEDICAL COMPANY RADIOFREQUENCY PERFORATION GENERATOR
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510(K) Number: K122278
Device Name: BAYLIS MEDICAL COMPANY RADIOFREQUENCY PERFORATION GENERATOR
Manufacturer: MEGHAL KHAKHAR
Device Classification Name: Electrosurgical, Cutting & Coagulation & Accessories
Regulation Number: GEI
Classification Product Code: 07/30/2012
Date Received: 11/07/2012
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: General & Plastic Surgery
Device Name: BAYLIS MEDICAL COMPANY RADIOFREQUENCY PERFORATION GENERATOR
Manufacturer: MEGHAL KHAKHAR
Device Classification Name: Electrosurgical, Cutting & Coagulation & Accessories
Regulation Number: GEI
Classification Product Code: 07/30/2012
Date Received: 11/07/2012
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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