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FDA 510(k)

KACEY INSULIN SYRINGE

K-Number: K033166 · 2003-12-12

ApplicantKacey, Inc.
Decision Date2003-12-12
Product CodeFMF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

KACEY INSULIN SYRINGE is the device name listed in this FDA 510(k) record. The listed applicant is Kacey, Inc.. It received FDA 510(k) clearance on 2003-12-12 under 510(k) number K033166. 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 KACEY INSULIN SYRINGE?

KACEY INSULIN SYRINGE is a medical device that received FDA 510(k) clearance on 2003-12-12. The listed applicant is Kacey, Inc.. The 510(k) number is K033166.

When did KACEY INSULIN SYRINGE receive FDA 510(k) clearance?

KACEY INSULIN SYRINGE received FDA 510(k) clearance on 2003-12-12, under 510(k) number K033166.

Who is the listed applicant for KACEY INSULIN SYRINGE?

The FDA 510(k) record lists Kacey, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for KACEY INSULIN SYRINGE?

The FDA product code for KACEY INSULIN SYRINGE is FMF.

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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.

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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.

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