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FDA 510(k)

TRIMETHOPRIM 5MCG. ANTIMICROBIAL DISK

K-Number: K812783 · 1981-10-23

ApplicantGeneral Diagnostics
Decision Date1981-10-23
Product CodeJTN
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

TRIMETHOPRIM 5MCG. ANTIMICROBIAL DISK is the device name listed in this FDA 510(k) record. The listed applicant is General Diagnostics. It received FDA 510(k) clearance on 1981-10-23 under 510(k) number K812783. 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 TRIMETHOPRIM 5MCG. ANTIMICROBIAL DISK?

TRIMETHOPRIM 5MCG. ANTIMICROBIAL DISK is a medical device that received FDA 510(k) clearance on 1981-10-23. The listed applicant is General Diagnostics. The 510(k) number is K812783.

When did TRIMETHOPRIM 5MCG. ANTIMICROBIAL DISK receive FDA 510(k) clearance?

TRIMETHOPRIM 5MCG. ANTIMICROBIAL DISK received FDA 510(k) clearance on 1981-10-23, under 510(k) number K812783.

Who is the listed applicant for TRIMETHOPRIM 5MCG. ANTIMICROBIAL DISK?

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 TRIMETHOPRIM 5MCG. ANTIMICROBIAL DISK?

The FDA product code for TRIMETHOPRIM 5MCG. ANTIMICROBIAL DISK is JTN.

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Other records listing General Diagnostics 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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