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FDA 510(k), K083594, EZ HSG CATHETER.FOAMSEAL CATHETER
FDA 510(k), K083594, EZ HSG CATHETER.FOAMSEAL CATHETER
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510(K) Number: K083594
Device Name: EZ HSG CATHETER.FOAMSEAL CATHETER
Manufacturer: OBG PRODUCTS
Device Classification Name: cannula, manipulator/injector, uterine
Regulation Number: 884.4530
Classification Product Code: LKF
Date Received: 12/05/2008
Decision Date: 07/21/2009
Regulation Medical Specialty: Obstetrics/Gynecology
Device Name: EZ HSG CATHETER.FOAMSEAL CATHETER
Manufacturer: OBG PRODUCTS
Device Classification Name: cannula, manipulator/injector, uterine
Regulation Number: 884.4530
Classification Product Code: LKF
Date Received: 12/05/2008
Decision Date: 07/21/2009
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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