FDA 510(k), K942823, MAHE INSTRUMENTS

FDA 510(k), K942823, MAHE INSTRUMENTS

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510(K) Number: K942823
Device Name: MAHE INSTRUMENTS
Manufacturer:
Device Classification Name: Electrosurgical Device
Regulation Number: 878.4400
Classification Product Code: DWG
Date Received: 06/14/1994
Decision Date: 12/05/1994
Regulation Medical Specialty: General & Plastic Surgery
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