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FDA 510(k)

CLEARVIEW HCG SERUM/URINE PROFESS PREG TEST, MODIF

K-Number: K914240 · 1991-10-25

ApplicantUnipath , Ltd.
Decision Date1991-10-25
Product CodeJHI
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

CLEARVIEW HCG SERUM/URINE PROFESS PREG TEST, MODIF is the device name listed in this FDA 510(k) record. The listed applicant is Unipath , Ltd.. It received FDA 510(k) clearance on 1991-10-25 under 510(k) number K914240. 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 CLEARVIEW HCG SERUM/URINE PROFESS PREG TEST, MODIF?

CLEARVIEW HCG SERUM/URINE PROFESS PREG TEST, MODIF is a medical device that received FDA 510(k) clearance on 1991-10-25. The listed applicant is Unipath , Ltd.. The 510(k) number is K914240.

When did CLEARVIEW HCG SERUM/URINE PROFESS PREG TEST, MODIF receive FDA 510(k) clearance?

CLEARVIEW HCG SERUM/URINE PROFESS PREG TEST, MODIF received FDA 510(k) clearance on 1991-10-25, under 510(k) number K914240.

Who is the listed applicant for CLEARVIEW HCG SERUM/URINE PROFESS PREG TEST, MODIF?

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

What is the FDA product code for CLEARVIEW HCG SERUM/URINE PROFESS PREG TEST, MODIF?

The FDA product code for CLEARVIEW HCG SERUM/URINE PROFESS PREG TEST, MODIF is JHI.

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Other records listing Unipath , Ltd. 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.

K061769E.P.T. CERTAINTY 1-STEP PREGNANCY TESTK060128CLEARBLUE EASY DIGITAL PREGNANCY TESTK051638INVERNESS MEDICAL TESTPACK + PLUS STREP A WITH OBCK050930E.P.T. CERTAINTY PREGNANCY TESTK042280FACT PLUS ONE-STEP PREGNANCY TEST KITK041404CLEARBLUE EASY EASY READ PREGNANCY TEST

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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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