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FDA 510(k)

GENERAL DIAGNOSTICS TICARCILLIN 75MCG SUSCEPT-DISK

K-Number: K850957 · 1985-05-01

ApplicantWarner-Lambert Co.
Decision Date1985-05-01
Product CodeJTN
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

GENERAL DIAGNOSTICS TICARCILLIN 75MCG SUSCEPT-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 1985-05-01 under 510(k) number K850957. 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 TICARCILLIN 75MCG SUSCEPT-DISK?

GENERAL DIAGNOSTICS TICARCILLIN 75MCG SUSCEPT-DISK is a medical device that received FDA 510(k) clearance on 1985-05-01. The listed applicant is Warner-Lambert Co.. The 510(k) number is K850957.

When did GENERAL DIAGNOSTICS TICARCILLIN 75MCG SUSCEPT-DISK receive FDA 510(k) clearance?

GENERAL DIAGNOSTICS TICARCILLIN 75MCG SUSCEPT-DISK received FDA 510(k) clearance on 1985-05-01, under 510(k) number K850957.

Who is the listed applicant for GENERAL DIAGNOSTICS TICARCILLIN 75MCG SUSCEPT-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 TICARCILLIN 75MCG SUSCEPT-DISK?

The FDA product code for GENERAL DIAGNOSTICS TICARCILLIN 75MCG SUSCEPT-DISK is JTN.

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Other records listing Warner-Lambert Co. as applicant

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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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