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FDA 510(k)

URIC ACID CATALOGE# 220-93/94/97

K-Number: K955496 · 1996-02-23

Decision Date1996-02-23
Product CodeKNK
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

URIC ACID CATALOGE# 220-93/94/97 is the device name listed in this FDA 510(k) record. The listed applicant is Diagnostic Chemicals , Ltd.. It received FDA 510(k) clearance on 1996-02-23 under 510(k) number K955496. 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 CATALOGE# 220-93/94/97?

URIC ACID CATALOGE# 220-93/94/97 is a medical device that received FDA 510(k) clearance on 1996-02-23. The listed applicant is Diagnostic Chemicals , Ltd.. The 510(k) number is K955496.

When did URIC ACID CATALOGE# 220-93/94/97 receive FDA 510(k) clearance?

URIC ACID CATALOGE# 220-93/94/97 received FDA 510(k) clearance on 1996-02-23, under 510(k) number K955496.

Who is the listed applicant for URIC ACID CATALOGE# 220-93/94/97?

The FDA 510(k) record lists Diagnostic Chemicals , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for URIC ACID CATALOGE# 220-93/94/97?

The FDA product code for URIC ACID CATALOGE# 220-93/94/97 is KNK.

Related Clinical Trials

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.

Other records listing Diagnostic Chemicals , Ltd. 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.

View all 66 devices →

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.

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.

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