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FDA 510(k), K152848, AUTOLAP SYSTEM
FDA 510(k), K152848, AUTOLAP SYSTEM
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510(K) Number: K152848
Device Name: AUTOLAP SYSTEM
Manufacturer: M.S.T Medical Surgery Technologies LTD
Device Classification Name: Laparoscope, General & Plastic Surgery
Regulation Number: 876.1500
Classification Product Code: GCJ
Date Received: 09/29/2015
Decision Date: 11/17/2015
Regulation Medical Specialty: Gastroenterology/Urology
Device Name: AUTOLAP SYSTEM
Manufacturer: M.S.T Medical Surgery Technologies LTD
Device Classification Name: Laparoscope, General & Plastic Surgery
Regulation Number: 876.1500
Classification Product Code: GCJ
Date Received: 09/29/2015
Decision Date: 11/17/2015
Regulation Medical Specialty: Gastroenterology/Urology
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks when the FOIA office is operating at regular capacity
NOTE: This document is not currently in our library. Upon purchase, we will request the document from the FDA FOIA office. Learn more about Fast-Track Requests here.
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