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FDA 510(k)

MODIFICATION TO E.P.T. PREGNANCY TEST

K-Number: K040329 · 2004-03-08

ApplicantUnipath , Ltd.
Decision Date2004-03-08
Product CodeLCX
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

MODIFICATION TO E.P.T. PREGNANCY TEST is the device name listed in this FDA 510(k) record. The listed applicant is Unipath , Ltd.. It received FDA 510(k) clearance on 2004-03-08 under 510(k) number K040329. The device is classified under product code LCX. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODIFICATION TO E.P.T. PREGNANCY TEST?

MODIFICATION TO E.P.T. PREGNANCY TEST is a medical device that received FDA 510(k) clearance on 2004-03-08. The listed applicant is Unipath , Ltd.. The 510(k) number is K040329.

When did MODIFICATION TO E.P.T. PREGNANCY TEST receive FDA 510(k) clearance?

MODIFICATION TO E.P.T. PREGNANCY TEST received FDA 510(k) clearance on 2004-03-08, under 510(k) number K040329.

Who is the listed applicant for MODIFICATION TO E.P.T. PREGNANCY TEST?

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 MODIFICATION TO E.P.T. PREGNANCY TEST?

The FDA product code for MODIFICATION TO E.P.T. PREGNANCY TEST is LCX.

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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: LCX)

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.

K251040MissLan® Early Detection Digital Pregnancy Test; MissLan® Early Result Digital Pregnancy TestGuangzhou Decheng Biotechnology Co., Ltd.K251053Shinetell PlusTM Digital Early Pregnancy TestHangzhou AllTest Biotech Co., Ltd.K250117FaStep Pregnancy Rapid Test Cassette; Fastep HCG Rapid Test CassetteAssure Tech., LLCK242135Synthgene Home Test HCG Test Strip; Synthgene Home Test HCG Test Cassette; Synthgene Home Test HCG Test MidstreamNanjing Synthgene Medical Technology Co., Ltd.K243573FaStep Early Pregnancy Rapid Test Strip; FaStep Early Pregnancy Rapid Test Cassette; FaStep Early Pregnancy Rapid Test MidstreamAssure Tech., LLCK241394iHealth® Early Pregnancy Test; iHealth® Early Pregnancy Test StripAndon Health 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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