FDA 510(k), K992760, SELECT-SUTTER MICRO BIPOLAR FORCEPS
FDA 510(k), K992760, SELECT-SUTTER MICRO BIPOLAR FORCEPS
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510(K) Number: K992760
Device Name: SELECT-SUTTER MICRO BIPOLAR FORCEPS
Manufacturer: SELECT MEDIZINTECHNIK HERMANN SUTTER GMBH
Device Classification Name: electrosurgical, cutting & coagulation & accessories
Regulation Number: 878.4400
Classification Product Code: GEI
Date Received: 08/17/1999
Decision Date: 10/25/1999
Regulation Medical Specialty: General & Plastic Surgery
Device Name: SELECT-SUTTER MICRO BIPOLAR FORCEPS
Manufacturer: SELECT MEDIZINTECHNIK HERMANN SUTTER GMBH
Device Classification Name: electrosurgical, cutting & coagulation & accessories
Regulation Number: 878.4400
Classification Product Code: GEI
Date Received: 08/17/1999
Decision Date: 10/25/1999
Regulation Medical Specialty: General & Plastic Surgery
- 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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