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FDA 510(k) K940466, TITANIUM BIPOLAR FORCEPS, by Radionics, Inc.

FDA 510(k) K940466, TITANIUM BIPOLAR FORCEPS, by Radionics, Inc.

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510(K) Number: K940466
Device Name: TITANIUM BIPOLAR FORCEPS
Manufacturer: Radionics, Inc.
Device Classification Name: electrosurgical, cutting & coagulation & accessories
Regulation Number: 878.4400
Classification Product Code: GEI
Date Received: 02/02/1994
Decision Date: 04/21/1994
Regulation Medical Specialty: General & Plastic Surgery
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