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FDA 510(k)

DIFFERENTIATION DISKS KANAMYCIN 1000 MCG

K-Number: K860565 · 1986-03-11

ApplicantDifco Laboratories, Inc.
Decision Date1986-03-11
Product CodeJTO
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

DIFFERENTIATION DISKS KANAMYCIN 1000 MCG 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 1986-03-11 under 510(k) number K860565. 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 KANAMYCIN 1000 MCG?

DIFFERENTIATION DISKS KANAMYCIN 1000 MCG is a medical device that received FDA 510(k) clearance on 1986-03-11. The listed applicant is Difco Laboratories, Inc.. The 510(k) number is K860565.

When did DIFFERENTIATION DISKS KANAMYCIN 1000 MCG receive FDA 510(k) clearance?

DIFFERENTIATION DISKS KANAMYCIN 1000 MCG received FDA 510(k) clearance on 1986-03-11, under 510(k) number K860565.

Who is the listed applicant for DIFFERENTIATION DISKS KANAMYCIN 1000 MCG?

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 KANAMYCIN 1000 MCG?

The FDA product code for DIFFERENTIATION DISKS KANAMYCIN 1000 MCG 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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