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FDA 510(k)

QUANTRX FEMALE FERTILITY TEST

K-Number: K070484 · 2007-10-22

ApplicantQuantrx Biomedical Corporation
Decision Date2007-10-22
Product CodeNGA
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

QUANTRX FEMALE FERTILITY TEST is the device name listed in this FDA 510(k) record. The listed applicant is Quantrx Biomedical Corporation. It received FDA 510(k) clearance on 2007-10-22 under 510(k) number K070484. The device is classified under product code NGA. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the QUANTRX FEMALE FERTILITY TEST?

QUANTRX FEMALE FERTILITY TEST is a medical device that received FDA 510(k) clearance on 2007-10-22. The listed applicant is Quantrx Biomedical Corporation. The 510(k) number is K070484.

When did QUANTRX FEMALE FERTILITY TEST receive FDA 510(k) clearance?

QUANTRX FEMALE FERTILITY TEST received FDA 510(k) clearance on 2007-10-22, under 510(k) number K070484.

Who is the listed applicant for QUANTRX FEMALE FERTILITY TEST?

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

What is the FDA product code for QUANTRX FEMALE FERTILITY TEST?

The FDA product code for QUANTRX FEMALE FERTILITY TEST is NGA.

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Other records listing Quantrx Biomedical Corporation 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.

K080436RAPIDSENSE DRUGS OF ABUSE COCAINE (COC) 300 DEVICE, MODEL 900-0052K080431RAPIDSENSE DRUGS OF ABUSE PHENCYCLIDINE (PCP) 25 DEVICE WITH MODELS 900-0054K080455RAPIDSENSE DRUGS OF ABUSE METHAMPHETAMINE (MET) 1000 DEVICE, MODEL 900-0050

Related Devices (Code: NGA)

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.

K032002FERTELL FEMALE FERTILITY TESTGenosis, Inc.

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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