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FDA 510(k), K833866, ACE/KYLE SELF TAPPING CANNULATED TITA
FDA 510(k), K833866, ACE/KYLE SELF TAPPING CANNULATED TITA
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510(K) Number: K833866
Device Name: ACE/KYLE SELF TAPPING CANNULATED TITA
Manufacturer: BUCKMAN CO., INC.
Device Classification Name: pump, nebulizer, electrically powered
Regulation Number: 874.5220
Classification Product Code: JPW
Date Received: 11/07/1983
Decision Date: 12/27/1983
Regulation Medical Specialty: Ear Nose & Throat
Device Name: ACE/KYLE SELF TAPPING CANNULATED TITA
Manufacturer: BUCKMAN CO., INC.
Device Classification Name: pump, nebulizer, electrically powered
Regulation Number: 874.5220
Classification Product Code: JPW
Date Received: 11/07/1983
Decision Date: 12/27/1983
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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