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FDA 510(k)

DOCUMENT(TM) URIC ACID LINEARITY TEST SET

K-Number: K893139 · 1989-07-20

ApplicantCasco Standards
Decision Date1989-07-20
Product CodeJIT
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

DOCUMENT(TM) URIC ACID LINEARITY TEST SET is the device name listed in this FDA 510(k) record. The listed applicant is Casco Standards. It received FDA 510(k) clearance on 1989-07-20 under 510(k) number K893139. The device is classified under product code JIT. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DOCUMENT(TM) URIC ACID LINEARITY TEST SET?

DOCUMENT(TM) URIC ACID LINEARITY TEST SET is a medical device that received FDA 510(k) clearance on 1989-07-20. The listed applicant is Casco Standards. The 510(k) number is K893139.

When did DOCUMENT(TM) URIC ACID LINEARITY TEST SET receive FDA 510(k) clearance?

DOCUMENT(TM) URIC ACID LINEARITY TEST SET received FDA 510(k) clearance on 1989-07-20, under 510(k) number K893139.

Who is the listed applicant for DOCUMENT(TM) URIC ACID LINEARITY TEST SET?

The FDA 510(k) record lists Casco Standards as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DOCUMENT(TM) URIC ACID LINEARITY TEST SET?

The FDA product code for DOCUMENT(TM) URIC ACID LINEARITY TEST SET is JIT.

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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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