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FDA 510(k)

VISUAL HCG PREGNANCY TEST

K-Number: K923376 · 1992-10-01

ApplicantTech-Co, Inc.
Decision Date1992-10-01
Product CodeJHI
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

VISUAL HCG PREGNANCY TEST is the device name listed in this FDA 510(k) record. The listed applicant is Tech-Co, Inc.. It received FDA 510(k) clearance on 1992-10-01 under 510(k) number K923376. The device is classified under product code JHI. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VISUAL HCG PREGNANCY TEST?

VISUAL HCG PREGNANCY TEST is a medical device that received FDA 510(k) clearance on 1992-10-01. The listed applicant is Tech-Co, Inc.. The 510(k) number is K923376.

When did VISUAL HCG PREGNANCY TEST receive FDA 510(k) clearance?

VISUAL HCG PREGNANCY TEST received FDA 510(k) clearance on 1992-10-01, under 510(k) number K923376.

Who is the listed applicant for VISUAL HCG PREGNANCY TEST?

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

What is the FDA product code for VISUAL HCG PREGNANCY TEST?

The FDA product code for VISUAL HCG PREGNANCY TEST is JHI.

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 Tech-Co, 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.

View all 36 devices →

Related Devices (Code: JHI)

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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