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FDA 510(k)

URIC ACID KIT, CODES 4825400 AND 4825050

K-Number: K890319 · 1989-04-12

ApplicantAmerican Research Products Co.
Decision Date1989-04-12
Product CodeKNK
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

URIC ACID KIT, CODES 4825400 AND 4825050 is the device name listed in this FDA 510(k) record. The listed applicant is American Research Products Co.. It received FDA 510(k) clearance on 1989-04-12 under 510(k) number K890319. The device is classified under product code KNK. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the URIC ACID KIT, CODES 4825400 AND 4825050?

URIC ACID KIT, CODES 4825400 AND 4825050 is a medical device that received FDA 510(k) clearance on 1989-04-12. The listed applicant is American Research Products Co.. The 510(k) number is K890319.

When did URIC ACID KIT, CODES 4825400 AND 4825050 receive FDA 510(k) clearance?

URIC ACID KIT, CODES 4825400 AND 4825050 received FDA 510(k) clearance on 1989-04-12, under 510(k) number K890319.

Who is the listed applicant for URIC ACID KIT, CODES 4825400 AND 4825050?

The FDA 510(k) record lists American Research Products Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for URIC ACID KIT, CODES 4825400 AND 4825050?

The FDA product code for URIC ACID KIT, CODES 4825400 AND 4825050 is KNK.

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Other records listing American Research Products Co. as applicant

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Related Devices (Code: KNK)

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.

K102568URIC ACID MODEL 3P39Abbott LaboratoriesK062862OLYMPUS URIC ACID REAGENT, MODEL OSR6X98Olympus America, Inc.K040467VITALAB URIC ACID REAGENTClinical Data, Inc.K031044ATAC PAK URIC ACID REAGENT AND ATAC CALIBRATORClinical Data, Inc.K022096URIC ACID ASSAY FOR THE ADVIA INTEGRATED MODULAR SYSTEMBayer Diagnostics Corp.K023550WIENER LAB URICOSTAT ENZIMATICO AA LIQUIDAWiener Laboratories Saic

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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