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FDA 510(k)

HYPODERMIC SYRINGE LUER LOK

K-Number: K901203 · 1990-06-06

ApplicantWare-Medics Glass Works, Inc.
Decision Date1990-06-06
Product CodeFMF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

HYPODERMIC SYRINGE LUER LOK is the device name listed in this FDA 510(k) record. The listed applicant is Ware-Medics Glass Works, Inc.. It received FDA 510(k) clearance on 1990-06-06 under 510(k) number K901203. 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 HYPODERMIC SYRINGE LUER LOK?

HYPODERMIC SYRINGE LUER LOK is a medical device that received FDA 510(k) clearance on 1990-06-06. The listed applicant is Ware-Medics Glass Works, Inc.. The 510(k) number is K901203.

When did HYPODERMIC SYRINGE LUER LOK receive FDA 510(k) clearance?

HYPODERMIC SYRINGE LUER LOK received FDA 510(k) clearance on 1990-06-06, under 510(k) number K901203.

Who is the listed applicant for HYPODERMIC SYRINGE LUER LOK?

The FDA 510(k) record lists Ware-Medics Glass Works, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for HYPODERMIC SYRINGE LUER LOK?

The FDA product code for HYPODERMIC SYRINGE LUER LOK 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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