Sonopet 1Q 3 7cm 1Q Large
K-Number: K223770 · 2023-02-16
Device Summary
Frequently Asked Questions
What is the Sonopet 1Q 3 7cm 1Q Large?
Sonopet 1Q 3 7cm 1Q Large is a medical device that received FDA 510(k) clearance on 2023-02-16. The listed applicant is Stryker Corporation. The 510(k) number is K223770.
When did Sonopet 1Q 3 7cm 1Q Large receive FDA 510(k) clearance?
Sonopet 1Q 3 7cm 1Q Large received FDA 510(k) clearance on 2023-02-16, under 510(k) number K223770.
Who is the listed applicant for Sonopet 1Q 3 7cm 1Q Large?
The FDA 510(k) record lists Stryker Corporation as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Sonopet 1Q 3 7cm 1Q Large?
The FDA product code for Sonopet 1Q 3 7cm 1Q Large is LFL.
Other records listing Stryker Corporation 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: LFL)
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.