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FDA 510(k)

MEZLOCILLIN 75MCG ANTIMICROB. SUSCEPT. D

K-Number: K812916 · 1981-11-06

ApplicantGeneral Diagnostics
Decision Date1981-11-06
Product CodeJTN
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

MEZLOCILLIN 75MCG ANTIMICROB. SUSCEPT. D is the device name listed in this FDA 510(k) record. The listed applicant is General Diagnostics. It received FDA 510(k) clearance on 1981-11-06 under 510(k) number K812916. 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 MEZLOCILLIN 75MCG ANTIMICROB. SUSCEPT. D?

MEZLOCILLIN 75MCG ANTIMICROB. SUSCEPT. D is a medical device that received FDA 510(k) clearance on 1981-11-06. The listed applicant is General Diagnostics. The 510(k) number is K812916.

When did MEZLOCILLIN 75MCG ANTIMICROB. SUSCEPT. D receive FDA 510(k) clearance?

MEZLOCILLIN 75MCG ANTIMICROB. SUSCEPT. D received FDA 510(k) clearance on 1981-11-06, under 510(k) number K812916.

Who is the listed applicant for MEZLOCILLIN 75MCG ANTIMICROB. SUSCEPT. D?

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

What is the FDA product code for MEZLOCILLIN 75MCG ANTIMICROB. SUSCEPT. D?

The FDA product code for MEZLOCILLIN 75MCG ANTIMICROB. SUSCEPT. D is 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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