Hummingbird Tympanostomy Tube System
K-Number: K221254 · 2022-07-27
ApplicantPreceptis Medical, Inc.
Decision Date2022-07-27
Product CodeETD
Advisory CommitteeEN
DecisionSubstantially Equivalent
Device Summary
Hummingbird Tympanostomy Tube System is a medical device manufactured by Preceptis Medical, Inc.. It received FDA 510(k) clearance on 2022-07-27 under approval number K221254. The device is classified under product code ETD. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Hummingbird Tympanostomy Tube System?
Hummingbird Tympanostomy Tube System is a medical device that received FDA 510(k) clearance on 2022-07-27. It is manufactured by Preceptis Medical, Inc.. The 510(k) number is K221254.
When was Hummingbird Tympanostomy Tube System approved by the FDA?
Hummingbird Tympanostomy Tube System received FDA 510(k) clearance on 2022-07-27, under approval number K221254.
What company makes Hummingbird Tympanostomy Tube System?
Hummingbird Tympanostomy Tube System is manufactured by Preceptis Medical, Inc..
What is the FDA product code for Hummingbird Tympanostomy Tube System?
The FDA product code for Hummingbird Tympanostomy Tube System is ETD.
Other Devices by Preceptis Medical, Inc.
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Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.