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FDA 510(k)

REUSABLE GLASS SYRINGES

K-Number: K011176 · 2001-08-10

Decision Date2001-08-10
Product CodeFMF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

REUSABLE GLASS SYRINGES is the device name listed in this FDA 510(k) record. The listed applicant is Lockett Medical Corp.. It received FDA 510(k) clearance on 2001-08-10 under 510(k) number K011176. 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 REUSABLE GLASS SYRINGES?

REUSABLE GLASS SYRINGES is a medical device that received FDA 510(k) clearance on 2001-08-10. The listed applicant is Lockett Medical Corp.. The 510(k) number is K011176.

When did REUSABLE GLASS SYRINGES receive FDA 510(k) clearance?

REUSABLE GLASS SYRINGES received FDA 510(k) clearance on 2001-08-10, under 510(k) number K011176.

Who is the listed applicant for REUSABLE GLASS SYRINGES?

The FDA 510(k) record lists Lockett Medical Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for REUSABLE GLASS SYRINGES?

The FDA product code for REUSABLE GLASS SYRINGES is FMF.

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 Lockett Medical Corp. 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.

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