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FDA 510(k)

FORA PNC100 DIGITAL PREGANCY TEST, TD-5301 PREGANCY TEST

K-Number: K103487 · 2011-10-04

ApplicantTaidoc Technology Corporation
Decision Date2011-10-04
Product CodeLCX
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

FORA PNC100 DIGITAL PREGANCY TEST, TD-5301 PREGANCY TEST is the device name listed in this FDA 510(k) record. The listed applicant is Taidoc Technology Corporation. It received FDA 510(k) clearance on 2011-10-04 under 510(k) number K103487. 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 FORA PNC100 DIGITAL PREGANCY TEST, TD-5301 PREGANCY TEST?

FORA PNC100 DIGITAL PREGANCY TEST, TD-5301 PREGANCY TEST is a medical device that received FDA 510(k) clearance on 2011-10-04. The listed applicant is Taidoc Technology Corporation. The 510(k) number is K103487.

When did FORA PNC100 DIGITAL PREGANCY TEST, TD-5301 PREGANCY TEST receive FDA 510(k) clearance?

FORA PNC100 DIGITAL PREGANCY TEST, TD-5301 PREGANCY TEST received FDA 510(k) clearance on 2011-10-04, under 510(k) number K103487.

Who is the listed applicant for FORA PNC100 DIGITAL PREGANCY TEST, TD-5301 PREGANCY TEST?

The FDA 510(k) record lists Taidoc Technology Corporation as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for FORA PNC100 DIGITAL PREGANCY TEST, TD-5301 PREGANCY TEST?

The FDA product code for FORA PNC100 DIGITAL PREGANCY TEST, TD-5301 PREGANCY TEST is LCX.

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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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