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FDA 510(k)

DIFFERENTIATION DISKS NITRATE

K-Number: K843521 · 1984-10-02

ApplicantDifco Laboratories, Inc.
Decision Date1984-10-02
Product CodeJTO
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

DIFFERENTIATION DISKS NITRATE 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 1984-10-02 under 510(k) number K843521. 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 DIFFERENTIATION DISKS NITRATE?

DIFFERENTIATION DISKS NITRATE is a medical device that received FDA 510(k) clearance on 1984-10-02. The listed applicant is Difco Laboratories, Inc.. The 510(k) number is K843521.

When did DIFFERENTIATION DISKS NITRATE receive FDA 510(k) clearance?

DIFFERENTIATION DISKS NITRATE received FDA 510(k) clearance on 1984-10-02, under 510(k) number K843521.

Who is the listed applicant for DIFFERENTIATION DISKS NITRATE?

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 DIFFERENTIATION DISKS NITRATE?

The FDA product code for DIFFERENTIATION DISKS NITRATE is JTO.

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Other records listing Difco Laboratories, Inc. 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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