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FDA 510(k)

CONCEIVE ONE-STEP PREGNANCY TEST

K-Number: K925096 · 1992-12-28

ApplicantQuidel Corp.
Decision Date1992-12-28
Product CodeLCX
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

CONCEIVE ONE-STEP PREGNANCY TEST is the device name listed in this FDA 510(k) record. The listed applicant is Quidel Corp.. It received FDA 510(k) clearance on 1992-12-28 under 510(k) number K925096. 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 CONCEIVE ONE-STEP PREGNANCY TEST?

CONCEIVE ONE-STEP PREGNANCY TEST is a medical device that received FDA 510(k) clearance on 1992-12-28. The listed applicant is Quidel Corp.. The 510(k) number is K925096.

When did CONCEIVE ONE-STEP PREGNANCY TEST receive FDA 510(k) clearance?

CONCEIVE ONE-STEP PREGNANCY TEST received FDA 510(k) clearance on 1992-12-28, under 510(k) number K925096.

Who is the listed applicant for CONCEIVE ONE-STEP PREGNANCY TEST?

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

What is the FDA product code for CONCEIVE ONE-STEP PREGNANCY TEST?

The FDA product code for CONCEIVE ONE-STEP PREGNANCY 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.

Other records listing Quidel Corp. 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.

View all 93 devices →

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.

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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