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FDA 510(k), K993900, COAGULATION ELECTRODE, MODEL 2000; RADIOFREQUENCY GENERATOR, MODEL 20-115
FDA 510(k), K993900, COAGULATION ELECTRODE, MODEL 2000; RADIOFREQUENCY GENERATOR, MODEL 20-115
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$149.00 USD
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510(K) Number: K993900
Device Name: COAGULATION ELECTRODE, MODEL 2000; RADIOFREQUENCY GENERATOR, MODEL 20-115
Manufacturer:
Device Classification Name: Bronchoscope (Flexible Or Rigid)
Regulation Number: 874.4680
Classification Product Code: EOQ
Date Received: 11/16/1999
Decision Date: 01/28/2000
Regulation Medical Specialty: Ear Nose & Throat
Device Name: COAGULATION ELECTRODE, MODEL 2000; RADIOFREQUENCY GENERATOR, MODEL 20-115
Manufacturer:
Device Classification Name: Bronchoscope (Flexible Or Rigid)
Regulation Number: 874.4680
Classification Product Code: EOQ
Date Received: 11/16/1999
Decision Date: 01/28/2000
Regulation Medical Specialty: Ear Nose & Throat
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