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FDA 510(k)

DESERET UNIVERSAL LUER LOCK

K-Number: K821525 · 1982-06-23

ApplicantWarner-Lambert Co.
Decision Date1982-06-23
Product CodeKGZ
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

DESERET UNIVERSAL LUER LOCK is the device name listed in this FDA 510(k) record. The listed applicant is Warner-Lambert Co.. It received FDA 510(k) clearance on 1982-06-23 under 510(k) number K821525. The device is classified under product code KGZ. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DESERET UNIVERSAL LUER LOCK?

DESERET UNIVERSAL LUER LOCK is a medical device that received FDA 510(k) clearance on 1982-06-23. The listed applicant is Warner-Lambert Co.. The 510(k) number is K821525.

When did DESERET UNIVERSAL LUER LOCK receive FDA 510(k) clearance?

DESERET UNIVERSAL LUER LOCK received FDA 510(k) clearance on 1982-06-23, under 510(k) number K821525.

Who is the listed applicant for DESERET UNIVERSAL LUER LOCK?

The FDA 510(k) record lists Warner-Lambert Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DESERET UNIVERSAL LUER LOCK?

The FDA product code for DESERET UNIVERSAL LUER LOCK is KGZ.

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Other records listing Warner-Lambert Co. 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.

K024160NEOSPORIN SCAR SOLUTIONK893452EXTRA STRENGTH EFFERGRIP DENTURE ADHESIVE CREAMK870584O.P.T.(TM) OVULATION PREDICTION TESTK861510MULTILUMEN VIAPIC CENTRAL LINE CATHETERK852967GENERAL DIAGNOSTICS' CEFTRIAXONE 30MCG SUSDEP DISKK852689GENERAL DIAGNOSTICS CEFTAZIDIME 30 MCG SUSC DISK

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Related Devices (Code: KGZ)

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.

K022306AART SILICONE TUBINGAesthetic and Reconstructive Technologies, Inc.K974295BYRON MEDICAL ASPIRATION AND INFILTRATION/IRRIGATION TUBINGByron MedicalK973183WOUND DRAINAGE HOLDERR & D Medical Products, Inc.K955433DURALASTIC SILICONE TUBINGAllied Biomedical Corp.K942315NAVARRE PERCUTANEOUS ACCESS SETNavarre Biomedical , Ltd.K896087PALESTRANT IRRIGATION AND DRAINAGE SETNorth American Instrument Corp.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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