FDA 510(k)

URI-VAL

K-Number: K843680 · 1985-03-29

Decision Date1985-03-29

Product CodeJMZ

Advisory CommitteeCH

DecisionSubstantially Equivalent

Device Summary

URI-VAL is the device name listed in this FDA 510(k) record. The listed applicant is Cenogenics Corp.. It received FDA 510(k) clearance on 1985-03-29 under 510(k) number K843680. The device is classified under product code JMZ. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the URI-VAL?

URI-VAL is a medical device that received FDA 510(k) clearance on 1985-03-29. The listed applicant is Cenogenics Corp.. The 510(k) number is K843680.

When did URI-VAL receive FDA 510(k) clearance?

URI-VAL received FDA 510(k) clearance on 1985-03-29, under 510(k) number K843680.

Who is the listed applicant for URI-VAL?

The FDA 510(k) record lists Cenogenics Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for URI-VAL?

The FDA product code for URI-VAL is JMZ.

Other records listing Cenogenics Corp. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K042641CHEMVIEW-10 K030533ACCUNATE ONE-STEP,ACCUNATE ONE-STEP CASSETTE, ACCUNATE-CHOICE, ACCUNATE HOME PREGNANCY TEST K992397ACCUNATE-ONE STEP, ACCUNATE-ONE STEP CASSETTE K894793MONODEX

Related Devices (Code: JMZ)

K844589OSMOLARITY STANDARDSRna Medical Corp.

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.