FDA 510(k)

LDH CLINI GEL KIT

K-Number: K791827 · 1979-10-01

Decision Date1979-10-01

Product CodeCFE

Advisory CommitteeCH

DecisionSubstantially Equivalent

Device Summary

LDH CLINI GEL KIT is the device name listed in this FDA 510(k) record. The listed applicant is Clinical Sciences, Inc.. It received FDA 510(k) clearance on 1979-10-01 under 510(k) number K791827. The device is classified under product code CFE. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LDH CLINI GEL KIT?

LDH CLINI GEL KIT is a medical device that received FDA 510(k) clearance on 1979-10-01. The listed applicant is Clinical Sciences, Inc.. The 510(k) number is K791827.

When did LDH CLINI GEL KIT receive FDA 510(k) clearance?

LDH CLINI GEL KIT received FDA 510(k) clearance on 1979-10-01, under 510(k) number K791827.

Who is the listed applicant for LDH CLINI GEL KIT?

The FDA 510(k) record lists Clinical Sciences, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LDH CLINI GEL KIT?

The FDA product code for LDH CLINI GEL KIT is CFE.

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Related Devices (Code: CFE)

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.