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FDA 510(k)

WINGED NEEDLE SETS WITH AN ANTINEEDLE STICK PROTECTOR

K-Number: K023917 · 2003-02-26

Decision Date2003-02-26
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

WINGED NEEDLE SETS WITH AN ANTINEEDLE STICK PROTECTOR is the device name listed in this FDA 510(k) record. The listed applicant is Kawasumi Laboratories, Inc.. It received FDA 510(k) clearance on 2003-02-26 under 510(k) number K023917. The device is classified under product code FPA. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the WINGED NEEDLE SETS WITH AN ANTINEEDLE STICK PROTECTOR?

WINGED NEEDLE SETS WITH AN ANTINEEDLE STICK PROTECTOR is a medical device that received FDA 510(k) clearance on 2003-02-26. The listed applicant is Kawasumi Laboratories, Inc.. The 510(k) number is K023917.

When did WINGED NEEDLE SETS WITH AN ANTINEEDLE STICK PROTECTOR receive FDA 510(k) clearance?

WINGED NEEDLE SETS WITH AN ANTINEEDLE STICK PROTECTOR received FDA 510(k) clearance on 2003-02-26, under 510(k) number K023917.

Who is the listed applicant for WINGED NEEDLE SETS WITH AN ANTINEEDLE STICK PROTECTOR?

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

What is the FDA product code for WINGED NEEDLE SETS WITH AN ANTINEEDLE STICK PROTECTOR?

The FDA product code for WINGED NEEDLE SETS WITH AN ANTINEEDLE STICK PROTECTOR is FPA.

Related Clinical Trials

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.

Other records listing Kawasumi Laboratories, Inc. 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.

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Related Devices (Code: FPA)

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.

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