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FDA 510(k), K920394, MEROCEL EPISTACIS KIT
FDA 510(k), K920394, MEROCEL EPISTACIS KIT
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510(K) Number: K920394
Device Name: MEROCEL EPISTACIS KIT
Manufacturer: DOUGLAS R VALENTINE
Device Classification Name: Balloon, Epistaxis
Regulation Number: EMX
Classification Product Code: 01/30/1992
Date Received: 03/18/1993
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: Ear Nose & Throat
Device Name: MEROCEL EPISTACIS KIT
Manufacturer: DOUGLAS R VALENTINE
Device Classification Name: Balloon, Epistaxis
Regulation Number: EMX
Classification Product Code: 01/30/1992
Date Received: 03/18/1993
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: Ear Nose & Throat
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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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