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FDA 510(k)

MINOCYCLINE 30 MCG. SENSITIVITY DISCS

K-Number: K802178 · 1980-10-10

ApplicantDifco Laboratories, Inc.
Decision Date1980-10-10
Product CodeJTN
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

MINOCYCLINE 30 MCG. SENSITIVITY DISCS is the device name listed in this FDA 510(k) record. The listed applicant is Difco Laboratories, Inc.. It received FDA 510(k) clearance on 1980-10-10 under 510(k) number K802178. 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 30 MCG. SENSITIVITY DISCS?

MINOCYCLINE 30 MCG. SENSITIVITY DISCS is a medical device that received FDA 510(k) clearance on 1980-10-10. The listed applicant is Difco Laboratories, Inc.. The 510(k) number is K802178.

When did MINOCYCLINE 30 MCG. SENSITIVITY DISCS receive FDA 510(k) clearance?

MINOCYCLINE 30 MCG. SENSITIVITY DISCS received FDA 510(k) clearance on 1980-10-10, under 510(k) number K802178.

Who is the listed applicant for MINOCYCLINE 30 MCG. SENSITIVITY DISCS?

The FDA 510(k) record lists Difco Laboratories, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MINOCYCLINE 30 MCG. SENSITIVITY DISCS?

The FDA product code for MINOCYCLINE 30 MCG. SENSITIVITY DISCS 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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