FDA 510(k), K061555, ANCHOR LAPARSCOPIC TISSUE RETIEVAL SYSTEM
FDA 510(k), K061555, ANCHOR LAPARSCOPIC TISSUE RETIEVAL SYSTEM
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510(K) Number: K061555
Device Name: ANCHOR LAPARSCOPIC TISSUE RETIEVAL SYSTEM
Manufacturer:
Device Classification Name: Laparoscope, General & Plastic Surgery
Regulation Number: 876.1500
Classification Product Code: GCJ
Date Received: 06/05/2006
Decision Date: 08/31/2006
Regulation Medical Specialty: Gastroenterology/Urology
Device Name: ANCHOR LAPARSCOPIC TISSUE RETIEVAL SYSTEM
Manufacturer:
Device Classification Name: Laparoscope, General & Plastic Surgery
Regulation Number: 876.1500
Classification Product Code: GCJ
Date Received: 06/05/2006
Decision Date: 08/31/2006
Regulation Medical Specialty: Gastroenterology/Urology