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FDA 510(k)

DIFCO OXIDASE DRYSLIDE

K-Number: K896398 · 1989-12-18

ApplicantDifco Laboratories, Inc.
Decision Date1989-12-18
Product CodeJTO
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

DIFCO OXIDASE DRYSLIDE 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 1989-12-18 under 510(k) number K896398. The device is classified under product code JTO. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DIFCO OXIDASE DRYSLIDE?

DIFCO OXIDASE DRYSLIDE is a medical device that received FDA 510(k) clearance on 1989-12-18. The listed applicant is Difco Laboratories, Inc.. The 510(k) number is K896398.

When did DIFCO OXIDASE DRYSLIDE receive FDA 510(k) clearance?

DIFCO OXIDASE DRYSLIDE received FDA 510(k) clearance on 1989-12-18, under 510(k) number K896398.

Who is the listed applicant for DIFCO OXIDASE DRYSLIDE?

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 DIFCO OXIDASE DRYSLIDE?

The FDA product code for DIFCO OXIDASE DRYSLIDE is JTO.

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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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