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FDA 510(k), K935442, MAHE INSTRUMENTS
FDA 510(k), K935442, MAHE INSTRUMENTS
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$149.00 USD
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510(K) Number: K935442
Device Name: MAHE INSTRUMENTS
Manufacturer:
Device Classification Name: Laparoscope, General & Plastic Surgery
Regulation Number: 876.1500
Classification Product Code: GCJ
Date Received: 11/12/1993
Decision Date: 03/14/1994
Regulation Medical Specialty: Gastroenterology/Urology
Device Name: MAHE INSTRUMENTS
Manufacturer:
Device Classification Name: Laparoscope, General & Plastic Surgery
Regulation Number: 876.1500
Classification Product Code: GCJ
Date Received: 11/12/1993
Decision Date: 03/14/1994
Regulation Medical Specialty: Gastroenterology/Urology
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