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FDA 510(k)

Insulin Syringe

K-Number: K233794 · 2024-03-06

Decision Date2024-03-06
Product CodeFMF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

Insulin Syringe is the device name listed in this FDA 510(k) record. The listed applicant is Spm Medicare Pvt. , Ltd.. It received FDA 510(k) clearance on 2024-03-06 under 510(k) number K233794. 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 Syringe?

Insulin Syringe is a medical device that received FDA 510(k) clearance on 2024-03-06. The listed applicant is Spm Medicare Pvt. , Ltd.. The 510(k) number is K233794.

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

Insulin Syringe received FDA 510(k) clearance on 2024-03-06, under 510(k) number K233794.

Who is the listed applicant for Insulin Syringe?

The FDA 510(k) record lists Spm Medicare Pvt. , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Insulin Syringe?

The FDA product code for Insulin Syringe is FMF.

Other records listing Spm Medicare Pvt. , Ltd. 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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