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FDA 510(k), K200952, Hummingbird Tympanostomy Tube System
FDA 510(k), K200952, Hummingbird Tympanostomy Tube System
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510(K) Number: K200952
Device Name: Hummingbird Tympanostomy Tube System
Manufacturer: Preceptis Medical, Inc
Device Classification Name: tube, tympanostomy
Regulation Number: 874.3880
Classification Product Code: ETD
Date Received: 04/09/2020
Decision Date: 06/05/2020
Regulation Medical Specialty: Ear Nose & Throat
Device Name: Hummingbird Tympanostomy Tube System
Manufacturer: Preceptis Medical, Inc
Device Classification Name: tube, tympanostomy
Regulation Number: 874.3880
Classification Product Code: ETD
Date Received: 04/09/2020
Decision Date: 06/05/2020
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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