Sonopet 1Q 3 7cm 1Q Large
K-Number: K223770 · 2023-02-16
ApplicantStryker Corporation
Decision Date2023-02-16
Product CodeLFL
DecisionSubstantially Equivalent
Device Summary
Sonopet 1Q 3 7cm 1Q Large is a medical device manufactured by Stryker Corporation. It received FDA 510(k) clearance on 2023-02-16 under approval number K223770. The device is classified under product code LFL. FDA Decision: Substantially Equivalent.
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. It is manufactured by Stryker Corporation. The 510(k) number is K223770.
When was Sonopet 1Q 3 7cm 1Q Large approved by the FDA?
Sonopet 1Q 3 7cm 1Q Large received FDA 510(k) clearance on 2023-02-16, under approval number K223770.
What company makes Sonopet 1Q 3 7cm 1Q Large?
Sonopet 1Q 3 7cm 1Q Large is manufactured by Stryker Corporation.
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.
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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.