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FDA 510(k)

URIC ACID, MODEL UA112-01

K-Number: K991247 · 1999-05-25

Decision Date1999-05-25
Product CodeKNK
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

URIC ACID, MODEL UA112-01 is the device name listed in this FDA 510(k) record. The listed applicant is A.P. Total Care, Inc.. It received FDA 510(k) clearance on 1999-05-25 under 510(k) number K991247. 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, MODEL UA112-01?

URIC ACID, MODEL UA112-01 is a medical device that received FDA 510(k) clearance on 1999-05-25. The listed applicant is A.P. Total Care, Inc.. The 510(k) number is K991247.

When did URIC ACID, MODEL UA112-01 receive FDA 510(k) clearance?

URIC ACID, MODEL UA112-01 received FDA 510(k) clearance on 1999-05-25, under 510(k) number K991247.

Who is the listed applicant for URIC ACID, MODEL UA112-01?

The FDA 510(k) record lists A.P. Total Care, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for URIC ACID, MODEL UA112-01?

The FDA product code for URIC ACID, MODEL UA112-01 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 A.P. Total Care, Inc. 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 18 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

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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