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FDA 510(k)

UNIMARK HCG COMBO PREGNANCY TEST

K-Number: K013194 · 2001-10-10

ApplicantBiotech Atlantic, Inc.
Decision Date2001-10-10
Product CodeJHI
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

UNIMARK HCG COMBO PREGNANCY TEST is the device name listed in this FDA 510(k) record. The listed applicant is Biotech Atlantic, Inc.. It received FDA 510(k) clearance on 2001-10-10 under 510(k) number K013194. 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 UNIMARK HCG COMBO PREGNANCY TEST?

UNIMARK HCG COMBO PREGNANCY TEST is a medical device that received FDA 510(k) clearance on 2001-10-10. The listed applicant is Biotech Atlantic, Inc.. The 510(k) number is K013194.

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

UNIMARK HCG COMBO PREGNANCY TEST received FDA 510(k) clearance on 2001-10-10, under 510(k) number K013194.

Who is the listed applicant for UNIMARK HCG COMBO PREGNANCY TEST?

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

What is the FDA product code for UNIMARK HCG COMBO PREGNANCY TEST?

The FDA product code for UNIMARK HCG COMBO PREGNANCY TEST is JHI.

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Other records listing Biotech Atlantic, 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.

K032992UNIMARK HOME PREGNANCY TEST DEVICEK960174UNIMARK MIDSTREAM PREGNANCY TEST STICKK941090UNISTEP HCG PREGNANCY TEST STRIP

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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