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FDA 510(k)

ACID REAGENT, URIC SINGLE VIAL

K-Number: K781996 · 1979-01-03

ApplicantCalbiochem-Behring Corp.
Decision Date1979-01-03
Product CodeCDO
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

ACID REAGENT, URIC SINGLE VIAL is the device name listed in this FDA 510(k) record. The listed applicant is Calbiochem-Behring Corp.. It received FDA 510(k) clearance on 1979-01-03 under 510(k) number K781996. The device is classified under product code CDO. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ACID REAGENT, URIC SINGLE VIAL?

ACID REAGENT, URIC SINGLE VIAL is a medical device that received FDA 510(k) clearance on 1979-01-03. The listed applicant is Calbiochem-Behring Corp.. The 510(k) number is K781996.

When did ACID REAGENT, URIC SINGLE VIAL receive FDA 510(k) clearance?

ACID REAGENT, URIC SINGLE VIAL received FDA 510(k) clearance on 1979-01-03, under 510(k) number K781996.

Who is the listed applicant for ACID REAGENT, URIC SINGLE VIAL?

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

What is the FDA product code for ACID REAGENT, URIC SINGLE VIAL?

The FDA product code for ACID REAGENT, URIC SINGLE VIAL is CDO.

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Related Devices (Code: CDO)

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.

K033278RANDOX URIC ACIDRandox Laboratories, Ltd.K992798SIGMA DIAGNOSTICS INFINITY URIC ACID REAGENT, MODELS 684-25, 684-100P, 684-500P, 684-2000P, 683-20, 683-100PSigma Diagnostics, Inc.K982251SIGMA DIAGNOSTICS INFINITY URIC ACID REAGENT KITSigma Diagnostics, Inc.K981766URIC ACIDAbbott LaboratoriesK981189URIC ACIDAbbott LaboratoriesK971485URIC ACID - INCORPORATING DYNAMIC STABILIZATION TECHNOLOGY - (DST)Trace America, Inc.

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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