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FDA 510(k)

EZ-HCG URINE(PREGNANCY TEST)

K-Number: K003856 · 2001-02-21

Decision Date2001-02-21
Product CodeJHI
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

EZ-HCG URINE(PREGNANCY TEST) is the device name listed in this FDA 510(k) record. The listed applicant is Biomerica, Inc.. It received FDA 510(k) clearance on 2001-02-21 under 510(k) number K003856. 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 EZ-HCG URINE(PREGNANCY TEST)?

EZ-HCG URINE(PREGNANCY TEST) is a medical device that received FDA 510(k) clearance on 2001-02-21. The listed applicant is Biomerica, Inc.. The 510(k) number is K003856.

When did EZ-HCG URINE(PREGNANCY TEST) receive FDA 510(k) clearance?

EZ-HCG URINE(PREGNANCY TEST) received FDA 510(k) clearance on 2001-02-21, under 510(k) number K003856.

Who is the listed applicant for EZ-HCG URINE(PREGNANCY TEST)?

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

What is the FDA product code for EZ-HCG URINE(PREGNANCY TEST)?

The FDA product code for EZ-HCG URINE(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 Biomerica, 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 10 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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