FDA 510(k), K993407, OHMEDA MEDICAL OMNIBED

FDA 510(k), K993407, OHMEDA MEDICAL OMNIBED

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510(K) Number: K993407
Device Name: OHMEDA MEDICAL OMNIBED
Manufacturer: OHMEDA MEDICAL
Device Classification Name: incubator, neonatal
Regulation Number: 880.5400
Classification Product Code: FMZ
Date Received: 10/08/1999
Decision Date: 01/05/2000
Regulation Medical Specialty: General Hospital
  • 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. Learn more about Fast-Track Requests here.

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