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FDA 510(k)

DIFFERENTIATION DISKS HIPPURATE

K-Number: K834581 · 1984-02-13

ApplicantDifco Laboratories, Inc.
Decision Date1984-02-13
Product CodeJTO
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

DIFFERENTIATION DISKS HIPPURATE 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 1984-02-13 under 510(k) number K834581. 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 HIPPURATE?

DIFFERENTIATION DISKS HIPPURATE is a medical device that received FDA 510(k) clearance on 1984-02-13. The listed applicant is Difco Laboratories, Inc.. The 510(k) number is K834581.

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

DIFFERENTIATION DISKS HIPPURATE received FDA 510(k) clearance on 1984-02-13, under 510(k) number K834581.

Who is the listed applicant for DIFFERENTIATION DISKS HIPPURATE?

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 HIPPURATE?

The FDA product code for DIFFERENTIATION DISKS HIPPURATE is JTO.

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Other records listing Difco Laboratories, Inc. as applicant

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Related Devices (Code: 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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