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FDA 510(k), K935947, HI-TOPS ELECTRODES 14-8000
FDA 510(k), K935947, HI-TOPS ELECTRODES 14-8000
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510(K) Number: K935947
Device Name: HI-TOPS ELECTRODES 14-8000
Manufacturer: W. J. MEDICAL INSTRUMENTS, INC.
Device Classification Name: coagulator-cutter, endoscopic, unipolar (and accessories)
Regulation Number: 884.4160
Classification Product Code: KNF
Date Received: 12/13/1993
Decision Date: 02/28/1994
Regulation Medical Specialty: Obstetrics/Gynecology
Device Name: HI-TOPS ELECTRODES 14-8000
Manufacturer: W. J. MEDICAL INSTRUMENTS, INC.
Device Classification Name: coagulator-cutter, endoscopic, unipolar (and accessories)
Regulation Number: 884.4160
Classification Product Code: KNF
Date Received: 12/13/1993
Decision Date: 02/28/1994
Regulation Medical Specialty: Obstetrics/Gynecology
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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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