FDA 510(k), K152802, Grasping Forceps
FDA 510(k), K152802, Grasping Forceps
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510(K) Number: K152802
Device Name: Grasping Forceps
Manufacturer: MICRO-TECH (NANJING) CO., LTD.
Device Classification Name: endoscopic grasping/cutting instrument, non-powered
Regulation Number: 876.1500
Classification Product Code: OCZ
Date Received: 09/28/2015
Decision Date: 01/21/2016
Regulation Medical Specialty: Gastroenterology/Urology
Device Name: Grasping Forceps
Manufacturer: MICRO-TECH (NANJING) CO., LTD.
Device Classification Name: endoscopic grasping/cutting instrument, non-powered
Regulation Number: 876.1500
Classification Product Code: OCZ
Date Received: 09/28/2015
Decision Date: 01/21/2016
Regulation Medical Specialty: Gastroenterology/Urology