Hypodermic Syringes & Needle
K-Number: K222925 · 2023-07-18
Device Summary
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. The listed applicant is Lifelong Meditech Private Limited. The 510(k) number is K222925.
When did Hypodermic Syringes & Needle receive FDA 510(k) clearance?
Hypodermic Syringes & Needle received FDA 510(k) clearance on 2023-07-18, under 510(k) number K222925.
Who is the listed applicant for Hypodermic Syringes & Needle?
The FDA 510(k) record lists Lifelong Meditech Private Limited as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Hypodermic Syringes & Needle?
The FDA product code for Hypodermic Syringes & Needle is FMF.
Other records listing Lifelong Meditech Private Limited 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: FMF)
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.