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FDA 510(k), K071973, EPLEY OMNIAX
FDA 510(k), K071973, EPLEY OMNIAX
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510(K) Number: K071973
Device Name: EPLEY OMNIAX
Manufacturer: VESTICON
Device Classification Name: apparatus, vestibular analysis
Regulation Number:
Classification Product Code: LXV
Date Received: 07/17/2007
Decision Date: 06/20/2008
Regulation Medical Specialty:
Device Name: EPLEY OMNIAX
Manufacturer: VESTICON
Device Classification Name: apparatus, vestibular analysis
Regulation Number:
Classification Product Code: LXV
Date Received: 07/17/2007
Decision Date: 06/20/2008
Regulation Medical Specialty:
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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. IMPORTANT: The FDA FOIA office operations are currently suspended. We are happy to make the request but do not know when we will receive a response. Learn more about Fast-Track Requests here.
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