1
/
of
0
FDA 510(k), K915075, NEBULIZER (DIRECT PATIENT INTERFACE)
FDA 510(k), K915075, NEBULIZER (DIRECT PATIENT INTERFACE)
Regular price
$89.00 USD
Regular price
Sale price
$89.00 USD
Unit price
/
per
510(K) Number: K915075
Device Name: NEBULIZER (DIRECT PATIENT INTERFACE)
Manufacturer: RUSSELL W.KING
Device Classification Name: Nebulizer (Direct Patient Interface)
Regulation Number: CAF
Classification Product Code: KXA
Date Received: 11/08/1991
Decision Date: 07/16/1992
Decision: Substantially Equivalent (SESE)
Regulation Medical Specialty: Anesthesiology
Device Name: NEBULIZER (DIRECT PATIENT INTERFACE)
Manufacturer: RUSSELL W.KING
Device Classification Name: Nebulizer (Direct Patient Interface)
Regulation Number: CAF
Classification Product Code: KXA
Date Received: 11/08/1991
Decision Date: 07/16/1992
Decision: Substantially Equivalent (SESE)
Regulation Medical Specialty: Anesthesiology
Couldn't load pickup availability
- 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.
View full details