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FDA 510(k)

QLT ABSOLUTE URINE-HCG PREGNANCY TEST

K-Number: K881806 · 1988-08-02

Decision Date1988-08-02
Product CodeJHI
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

QLT ABSOLUTE URINE-HCG PREGNANCY TEST is the device name listed in this FDA 510(k) record. The listed applicant is Quadra Logic Technologies, Inc.. It received FDA 510(k) clearance on 1988-08-02 under 510(k) number K881806. The device is classified under product code JHI. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the QLT ABSOLUTE URINE-HCG PREGNANCY TEST?

QLT ABSOLUTE URINE-HCG PREGNANCY TEST is a medical device that received FDA 510(k) clearance on 1988-08-02. The listed applicant is Quadra Logic Technologies, Inc.. The 510(k) number is K881806.

When did QLT ABSOLUTE URINE-HCG PREGNANCY TEST receive FDA 510(k) clearance?

QLT ABSOLUTE URINE-HCG PREGNANCY TEST received FDA 510(k) clearance on 1988-08-02, under 510(k) number K881806.

Who is the listed applicant for QLT ABSOLUTE URINE-HCG PREGNANCY TEST?

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

What is the FDA product code for QLT ABSOLUTE URINE-HCG PREGNANCY TEST?

The FDA product code for QLT ABSOLUTE URINE-HCG PREGNANCY TEST is JHI.

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.

Related Devices (Code: JHI)

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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