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FDA 510(k)

GENERAL DIAGNOSTICS CEFTAZIDIME 30 MCG SUSC DISK

K-Number: K852689 · 1985-08-19

ApplicantWarner-Lambert Co.
Decision Date1985-08-19
Product CodeJTN
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

GENERAL DIAGNOSTICS CEFTAZIDIME 30 MCG SUSC DISK 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 1985-08-19 under 510(k) number K852689. The device is classified under product code JTN. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GENERAL DIAGNOSTICS CEFTAZIDIME 30 MCG SUSC DISK?

GENERAL DIAGNOSTICS CEFTAZIDIME 30 MCG SUSC DISK is a medical device that received FDA 510(k) clearance on 1985-08-19. The listed applicant is Warner-Lambert Co.. The 510(k) number is K852689.

When did GENERAL DIAGNOSTICS CEFTAZIDIME 30 MCG SUSC DISK receive FDA 510(k) clearance?

GENERAL DIAGNOSTICS CEFTAZIDIME 30 MCG SUSC DISK received FDA 510(k) clearance on 1985-08-19, under 510(k) number K852689.

Who is the listed applicant for GENERAL DIAGNOSTICS CEFTAZIDIME 30 MCG SUSC DISK?

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 GENERAL DIAGNOSTICS CEFTAZIDIME 30 MCG SUSC DISK?

The FDA product code for GENERAL DIAGNOSTICS CEFTAZIDIME 30 MCG SUSC DISK is JTN.

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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 DISKK852843GENERAL DIAGNOSTICS COAG-A-MATE XC

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Related Devices (Code: JTN)

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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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