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FDA 510(k)

MINOCYCLINE 30MCG ANTIMICROBIAL SUS. DSK

K-Number: K812994 · 1981-12-17

ApplicantGeneral Diagnostics
Decision Date1981-12-17
Product CodeJTN
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

MINOCYCLINE 30MCG ANTIMICROBIAL SUS. DSK is the device name listed in this FDA 510(k) record. The listed applicant is General Diagnostics. It received FDA 510(k) clearance on 1981-12-17 under 510(k) number K812994. 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 MINOCYCLINE 30MCG ANTIMICROBIAL SUS. DSK?

MINOCYCLINE 30MCG ANTIMICROBIAL SUS. DSK is a medical device that received FDA 510(k) clearance on 1981-12-17. The listed applicant is General Diagnostics. The 510(k) number is K812994.

When did MINOCYCLINE 30MCG ANTIMICROBIAL SUS. DSK receive FDA 510(k) clearance?

MINOCYCLINE 30MCG ANTIMICROBIAL SUS. DSK received FDA 510(k) clearance on 1981-12-17, under 510(k) number K812994.

Who is the listed applicant for MINOCYCLINE 30MCG ANTIMICROBIAL SUS. DSK?

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 MINOCYCLINE 30MCG ANTIMICROBIAL SUS. DSK?

The FDA product code for MINOCYCLINE 30MCG ANTIMICROBIAL SUS. DSK is JTN.

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Other records listing General Diagnostics as applicant

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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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