FDA 510(k), K942821, MAHE INSTRUMENTS
FDA 510(k), K942821, MAHE INSTRUMENTS
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510(K) Number: K942821
Device Name: MAHE INSTRUMENTS
Manufacturer:
Device Classification Name: Electrosurgical, Cutting & Coagulation & Accessories
Regulation Number: 878.4400
Classification Product Code: GEI
Date Received: 06/14/1994
Decision Date: 11/02/1994
Regulation Medical Specialty: General & Plastic Surgery
Device Name: MAHE INSTRUMENTS
Manufacturer:
Device Classification Name: Electrosurgical, Cutting & Coagulation & Accessories
Regulation Number: 878.4400
Classification Product Code: GEI
Date Received: 06/14/1994
Decision Date: 11/02/1994
Regulation Medical Specialty: General & Plastic Surgery