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FDA 510(k)

TIMENTIN 85MCG SENSITIVITY DISC

K-Number: K852423 · 1985-07-16

ApplicantDifco Laboratories, Inc.
Decision Date1985-07-16
Product Code
DecisionSubstantially Equivalent

Device Summary

TIMENTIN 85MCG SENSITIVITY DISC 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 1985-07-16 under 510(k) number K852423. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TIMENTIN 85MCG SENSITIVITY DISC?

TIMENTIN 85MCG SENSITIVITY DISC is a medical device that received FDA 510(k) clearance on 1985-07-16. The listed applicant is Difco Laboratories, Inc.. The 510(k) number is K852423.

When did TIMENTIN 85MCG SENSITIVITY DISC receive FDA 510(k) clearance?

TIMENTIN 85MCG SENSITIVITY DISC received FDA 510(k) clearance on 1985-07-16, under 510(k) number K852423.

Who is the listed applicant for TIMENTIN 85MCG SENSITIVITY DISC?

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

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Other records listing Difco Laboratories, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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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