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FDA 510(k)

DIFFERENTIATION DISKS PENICILLIN G 2 UNITS

K-Number: K860561 · 1986-03-11

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

Device Summary

DIFFERENTIATION DISKS PENICILLIN G 2 UNITS 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 K860561. 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 PENICILLIN G 2 UNITS?

DIFFERENTIATION DISKS PENICILLIN G 2 UNITS 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 K860561.

When did DIFFERENTIATION DISKS PENICILLIN G 2 UNITS receive FDA 510(k) clearance?

DIFFERENTIATION DISKS PENICILLIN G 2 UNITS received FDA 510(k) clearance on 1986-03-11, under 510(k) number K860561.

Who is the listed applicant for DIFFERENTIATION DISKS PENICILLIN G 2 UNITS?

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 PENICILLIN G 2 UNITS?

The FDA product code for DIFFERENTIATION DISKS PENICILLIN G 2 UNITS is JTO.

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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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