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FDA 510(k)

CARDS(TM) - EARLY PREGNANCY TEST

K-Number: K863341 · 1987-01-14

ApplicantPacific Biotech, Inc.
Decision Date1987-01-14
Product CodeLCX
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

CARDS(TM) - EARLY PREGNANCY TEST is the device name listed in this FDA 510(k) record. The listed applicant is Pacific Biotech, Inc.. It received FDA 510(k) clearance on 1987-01-14 under 510(k) number K863341. 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 CARDS(TM) - EARLY PREGNANCY TEST?

CARDS(TM) - EARLY PREGNANCY TEST is a medical device that received FDA 510(k) clearance on 1987-01-14. The listed applicant is Pacific Biotech, Inc.. The 510(k) number is K863341.

When did CARDS(TM) - EARLY PREGNANCY TEST receive FDA 510(k) clearance?

CARDS(TM) - EARLY PREGNANCY TEST received FDA 510(k) clearance on 1987-01-14, under 510(k) number K863341.

Who is the listed applicant for CARDS(TM) - EARLY PREGNANCY TEST?

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

What is the FDA product code for CARDS(TM) - EARLY PREGNANCY TEST?

The FDA product code for CARDS(TM) - EARLY PREGNANCY TEST is LCX.

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Other records listing Pacific Biotech, 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.

K924461STREP A NEGATIVE CONTROLK902510CARDS O.S. MONOK896482PERFECT(TM) ONE STEP EARLY PREGNANCY TEST KITK896221CARDS O.S.(TM) STREP AK895390CARDS O.S. (TM) HCG-URINEK891770HCG IRMA II

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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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