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FDA 510(k)

UC QIK PREGNANCY TEST

K-Number: K926500 · 1993-06-07

ApplicantEucardio Laboratory, Inc.
Decision Date1993-06-07
Product CodeJHI
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

UC QIK PREGNANCY TEST is the device name listed in this FDA 510(k) record. The listed applicant is Eucardio Laboratory, Inc.. It received FDA 510(k) clearance on 1993-06-07 under 510(k) number K926500. 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 UC QIK PREGNANCY TEST?

UC QIK PREGNANCY TEST is a medical device that received FDA 510(k) clearance on 1993-06-07. The listed applicant is Eucardio Laboratory, Inc.. The 510(k) number is K926500.

When did UC QIK PREGNANCY TEST receive FDA 510(k) clearance?

UC QIK PREGNANCY TEST received FDA 510(k) clearance on 1993-06-07, under 510(k) number K926500.

Who is the listed applicant for UC QIK PREGNANCY TEST?

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

What is the FDA product code for UC QIK PREGNANCY TEST?

The FDA product code for UC QIK PREGNANCY TEST is JHI.

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Other records listing Eucardio Laboratory, 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.

K942464UC QIK 1-STEP HCG TESTK904137UC IMU BK904125UC IMU A

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.

K262299Instant-View® hCG Combo II Cassette TestAlfa Scientific Designs, Inc.K241919Innovita HCG Pregnancy Rapid Combo TestInnovita (Tangshan) Biological Technology Co., Ltd.K203272Alltest Pregnancy Rapid Combo Test CassetteHangzhou AllTest Biotech Co., Ltd.K172322Atellica IM Total hCG (ThCG)Siemens Healthcare Diagnostics, Inc.K172257TrueDX hCG Early Result Pregnancy Test (Midstream Format), TrueDX hCG Early Result Pregnancy Test (Cassette Format), VeriClear Early Result Pregnancy Test (Midstream Format), VeriClear Early Result Pregnancy Test (Cassette Format)True Diagnostics, Inc.K152768Assure Tech hCG Pregnancy Serum/Urine Combo Test Cassette, Assure Tech hCG Pregnancy Serum/Urine Combo Test StripAssure Tech. Co., Ltd.

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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