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FDA 510(k)

QUANTITATE URIC ACID VERIFIER SET

K-Number: K944453 · 1994-11-22

ApplicantBeckman Instruments, Inc.
Decision Date1994-11-22
Product CodeJJX
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

QUANTITATE URIC ACID VERIFIER SET is the device name listed in this FDA 510(k) record. The listed applicant is Beckman Instruments, Inc.. It received FDA 510(k) clearance on 1994-11-22 under 510(k) number K944453. The device is classified under product code JJX. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the QUANTITATE URIC ACID VERIFIER SET?

QUANTITATE URIC ACID VERIFIER SET is a medical device that received FDA 510(k) clearance on 1994-11-22. The listed applicant is Beckman Instruments, Inc.. The 510(k) number is K944453.

When did QUANTITATE URIC ACID VERIFIER SET receive FDA 510(k) clearance?

QUANTITATE URIC ACID VERIFIER SET received FDA 510(k) clearance on 1994-11-22, under 510(k) number K944453.

Who is the listed applicant for QUANTITATE URIC ACID VERIFIER SET?

The FDA 510(k) record lists Beckman Instruments, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for QUANTITATE URIC ACID VERIFIER SET?

The FDA product code for QUANTITATE URIC ACID VERIFIER SET is JJX.

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Related Devices (Code: JJX)

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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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