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FDA 510(k)

ANSWER QUICK AND SIMPLE AT-HOME PREGNANCY TEST

K-Number: K904782 · 1990-12-06

Decision Date1990-12-06
Product CodeLCX
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

ANSWER QUICK AND SIMPLE AT-HOME PREGNANCY TEST is the device name listed in this FDA 510(k) record. The listed applicant is Carter Products. It received FDA 510(k) clearance on 1990-12-06 under 510(k) number K904782. 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 ANSWER QUICK AND SIMPLE AT-HOME PREGNANCY TEST?

ANSWER QUICK AND SIMPLE AT-HOME PREGNANCY TEST is a medical device that received FDA 510(k) clearance on 1990-12-06. The listed applicant is Carter Products. The 510(k) number is K904782.

When did ANSWER QUICK AND SIMPLE AT-HOME PREGNANCY TEST receive FDA 510(k) clearance?

ANSWER QUICK AND SIMPLE AT-HOME PREGNANCY TEST received FDA 510(k) clearance on 1990-12-06, under 510(k) number K904782.

Who is the listed applicant for ANSWER QUICK AND SIMPLE AT-HOME PREGNANCY TEST?

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

What is the FDA product code for ANSWER QUICK AND SIMPLE AT-HOME PREGNANCY TEST?

The FDA product code for ANSWER QUICK AND SIMPLE AT-HOME 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 Carter Products 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 20 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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