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FDA 510(k)

Insulin Syringes

K-Number: K242434 · 2024-12-24

Decision Date2024-12-24
Product CodeFMF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

Insulin Syringes is the device name listed in this FDA 510(k) record. The listed applicant is Chirana T. Injecta. It received FDA 510(k) clearance on 2024-12-24 under 510(k) number K242434. 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 Insulin Syringes?

Insulin Syringes is a medical device that received FDA 510(k) clearance on 2024-12-24. The listed applicant is Chirana T. Injecta. The 510(k) number is K242434.

When did Insulin Syringes receive FDA 510(k) clearance?

Insulin Syringes received FDA 510(k) clearance on 2024-12-24, under 510(k) number K242434.

Who is the listed applicant for Insulin Syringes?

The FDA 510(k) record lists Chirana T. Injecta as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Insulin Syringes?

The FDA product code for Insulin Syringes is FMF.

Other records listing Chirana T. Injecta 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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.