Hummingbird Tympanostomy Tube System
K-Number: K221254 · 2022-07-27
Device Summary
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. The listed applicant is Preceptis Medical, Inc.. The 510(k) number is K221254.
When did Hummingbird Tympanostomy Tube System receive FDA 510(k) clearance?
Hummingbird Tympanostomy Tube System received FDA 510(k) clearance on 2022-07-27, under 510(k) number K221254.
Who is the listed applicant for Hummingbird Tympanostomy Tube System?
The FDA 510(k) record lists Preceptis Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Hummingbird Tympanostomy Tube System?
The FDA product code for Hummingbird Tympanostomy Tube System is ETD.
Other records listing Preceptis Medical, Inc. as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: ETD)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
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.