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FDA 510(k)

PREGNA/TEST

K-Number: K853269 · 1985-10-03

ApplicantModern Diagnostics, Inc.
Decision Date1985-10-03
Product CodeLCX
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

PREGNA/TEST is the device name listed in this FDA 510(k) record. The listed applicant is Modern Diagnostics, Inc.. It received FDA 510(k) clearance on 1985-10-03 under 510(k) number K853269. 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 PREGNA/TEST?

PREGNA/TEST is a medical device that received FDA 510(k) clearance on 1985-10-03. The listed applicant is Modern Diagnostics, Inc.. The 510(k) number is K853269.

When did PREGNA/TEST receive FDA 510(k) clearance?

PREGNA/TEST received FDA 510(k) clearance on 1985-10-03, under 510(k) number K853269.

Who is the listed applicant for PREGNA/TEST?

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

What is the FDA product code for PREGNA/TEST?

The FDA product code for PREGNA/TEST is LCX.

Related Clinical Trials

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.

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Other records listing Modern Diagnostics, 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.

K853258BETA-HCG MICROTITER PREGNANCY TESTK853006HUMAN CHORIONIC GONAD TEST SYS FOR EARLY PREGNANCYK852840ENZYME ANTINUCLEAR ANTIBODY SCREENING TESTK851369ANTINUCLEAR ANTIBODY TEST KIT

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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