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FDA 510(k)

DIFFERENTIATION DISKS BILE ESCULIN

K-Number: K843364 · 1984-09-07

ApplicantDifco Laboratories, Inc.
Decision Date1984-09-07
Product CodeJSF
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

DIFFERENTIATION DISKS BILE ESCULIN 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 1984-09-07 under 510(k) number K843364. The device is classified under product code JSF. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DIFFERENTIATION DISKS BILE ESCULIN?

DIFFERENTIATION DISKS BILE ESCULIN is a medical device that received FDA 510(k) clearance on 1984-09-07. The listed applicant is Difco Laboratories, Inc.. The 510(k) number is K843364.

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

DIFFERENTIATION DISKS BILE ESCULIN received FDA 510(k) clearance on 1984-09-07, under 510(k) number K843364.

Who is the listed applicant for DIFFERENTIATION DISKS BILE ESCULIN?

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 BILE ESCULIN?

The FDA product code for DIFFERENTIATION DISKS BILE ESCULIN is JSF.

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Related Devices (Code: JSF)

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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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