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FDA 510(k), K170784, PNEUMOCLEAR
FDA 510(k), K170784, PNEUMOCLEAR
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510(K) Number: K170784
Device Name: PNEUMOCLEAR
Manufacturer: W.O.M World Of Medicine GmbH
Device Classification Name: insufflator, laparoscopic
Regulation Number: 884.1730
Classification Product Code: HIF
Date Received: 03/15/2017
Decision Date: 05/15/2017
Regulation Medical Specialty: Obstetrics/Gynecology
Device Name: PNEUMOCLEAR
Manufacturer: W.O.M World Of Medicine GmbH
Device Classification Name: insufflator, laparoscopic
Regulation Number: 884.1730
Classification Product Code: HIF
Date Received: 03/15/2017
Decision Date: 05/15/2017
Regulation Medical Specialty: Obstetrics/Gynecology
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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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