FDA 510(k), K102219, SOCORRO SMI TUNNEL RELEASE DEVICE
FDA 510(k), K102219, SOCORRO SMI TUNNEL RELEASE DEVICE
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$149.00 USD
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$149.00 USD
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510(K) Number: K102219
Device Name: SOCORRO SMI TUNNEL RELEASE DEVICE
Manufacturer:
Device Classification Name: Laparoscope, General & Plastic Surgery
Regulation Number: 876.1500
Classification Product Code: GCJ
Date Received: 08/06/2010
Decision Date: 09/24/2010
Regulation Medical Specialty: Gastroenterology/Urology
Device Name: SOCORRO SMI TUNNEL RELEASE DEVICE
Manufacturer:
Device Classification Name: Laparoscope, General & Plastic Surgery
Regulation Number: 876.1500
Classification Product Code: GCJ
Date Received: 08/06/2010
Decision Date: 09/24/2010
Regulation Medical Specialty: Gastroenterology/Urology