Hypodermic Syringes & Needle
K-Number: K222925 · 2023-07-18
ApplicantLifelong Meditech Private Limited
Decision Date2023-07-18
Product CodeFMF
Advisory CommitteeHO
DecisionSubstantially Equivalent
Device Summary
Hypodermic Syringes & Needle is a medical device manufactured by Lifelong Meditech Private Limited. It received FDA 510(k) clearance on 2023-07-18 under approval number K222925. The device is classified under product code FMF. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Hypodermic Syringes & Needle?
Hypodermic Syringes & Needle is a medical device that received FDA 510(k) clearance on 2023-07-18. It is manufactured by Lifelong Meditech Private Limited. The 510(k) number is K222925.
When was Hypodermic Syringes & Needle approved by the FDA?
Hypodermic Syringes & Needle received FDA 510(k) clearance on 2023-07-18, under approval number K222925.
What company makes Hypodermic Syringes & Needle?
Hypodermic Syringes & Needle is manufactured by Lifelong Meditech Private Limited.
What is the FDA product code for Hypodermic Syringes & Needle?
The FDA product code for Hypodermic Syringes & Needle is FMF.
Related Clinical Trials
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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.