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FDA 510(k)

POLY STAT SERUM/URINE HCG TEST

K-Number: K030430 · 2003-04-18

ApplicantAlidex, Inc.
Decision Date2003-04-18
Product CodeJHI
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

POLY STAT SERUM/URINE HCG TEST is the device name listed in this FDA 510(k) record. The listed applicant is Alidex, Inc.. It received FDA 510(k) clearance on 2003-04-18 under 510(k) number K030430. 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 POLY STAT SERUM/URINE HCG TEST?

POLY STAT SERUM/URINE HCG TEST is a medical device that received FDA 510(k) clearance on 2003-04-18. The listed applicant is Alidex, Inc.. The 510(k) number is K030430.

When did POLY STAT SERUM/URINE HCG TEST receive FDA 510(k) clearance?

POLY STAT SERUM/URINE HCG TEST received FDA 510(k) clearance on 2003-04-18, under 510(k) number K030430.

Who is the listed applicant for POLY STAT SERUM/URINE HCG TEST?

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

What is the FDA product code for POLY STAT SERUM/URINE HCG TEST?

The FDA product code for POLY STAT SERUM/URINE HCG 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.

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Other records listing Alidex, 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.

K021386POLY STAT HCG DIPSTICK TEST

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.

K262299Instant-View® hCG Combo II Cassette TestAlfa Scientific Designs, Inc.K241919Innovita HCG Pregnancy Rapid Combo TestInnovita (Tangshan) Biological Technology Co., Ltd.K203272Alltest Pregnancy Rapid Combo Test CassetteHangzhou AllTest Biotech Co., Ltd.K172322Atellica IM Total hCG (ThCG)Siemens Healthcare Diagnostics, Inc.K172257TrueDX hCG Early Result Pregnancy Test (Midstream Format), TrueDX hCG Early Result Pregnancy Test (Cassette Format), VeriClear Early Result Pregnancy Test (Midstream Format), VeriClear Early Result Pregnancy Test (Cassette Format)True Diagnostics, Inc.K152768Assure Tech hCG Pregnancy Serum/Urine Combo Test Cassette, Assure Tech hCG Pregnancy Serum/Urine Combo Test StripAssure Tech. Co., Ltd.

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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