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FDA 510(k), K140662, FLEX ENDOSCOPIC INSTRUMENTS
FDA 510(k), K140662, FLEX ENDOSCOPIC INSTRUMENTS
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510(K) Number: K140662
Device Name: FLEX ENDOSCOPIC INSTRUMENTS
Manufacturer: DESIGN STANDARDS CORP.
Device Classification Name: laparoscope, general & plastic surgery
Regulation Number: 876.1500
Classification Product Code: GCJ
Date Received: 03/14/2014
Decision Date: 06/11/2014
Regulation Medical Specialty: Gastroenterology/Urology
Device Name: FLEX ENDOSCOPIC INSTRUMENTS
Manufacturer: DESIGN STANDARDS CORP.
Device Classification Name: laparoscope, general & plastic surgery
Regulation Number: 876.1500
Classification Product Code: GCJ
Date Received: 03/14/2014
Decision Date: 06/11/2014
Regulation Medical Specialty: Gastroenterology/Urology
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks
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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