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FDA 510(k)

QUANTEX ASO-CRP-RP CONTROL II

K-Number: K984437 · 1999-02-02

ApplicantInstrumentation Laboratory CO
Decision Date1999-02-02
Product CodeJJT
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

QUANTEX ASO-CRP-RP CONTROL II is the device name listed in this FDA 510(k) record. The listed applicant is Instrumentation Laboratory CO. It received FDA 510(k) clearance on 1999-02-02 under 510(k) number K984437. The device is classified under product code JJT. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the QUANTEX ASO-CRP-RP CONTROL II?

QUANTEX ASO-CRP-RP CONTROL II is a medical device that received FDA 510(k) clearance on 1999-02-02. The listed applicant is Instrumentation Laboratory CO. The 510(k) number is K984437.

When did QUANTEX ASO-CRP-RP CONTROL II receive FDA 510(k) clearance?

QUANTEX ASO-CRP-RP CONTROL II received FDA 510(k) clearance on 1999-02-02, under 510(k) number K984437.

Who is the listed applicant for QUANTEX ASO-CRP-RP CONTROL II?

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

What is the FDA product code for QUANTEX ASO-CRP-RP CONTROL II?

The FDA product code for QUANTEX ASO-CRP-RP CONTROL II is JJT.

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Related Devices (Code: JJT)

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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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