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FDA 510(k)

COATED TUBE HCG IMMUNOASSAY HCG

K-Number: K841023 · 1984-05-01

ApplicantVentrex Laboratories, Inc.
Decision Date1984-05-01
Product CodeJHI
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

COATED TUBE HCG IMMUNOASSAY HCG is the device name listed in this FDA 510(k) record. The listed applicant is Ventrex Laboratories, Inc.. It received FDA 510(k) clearance on 1984-05-01 under 510(k) number K841023. 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 COATED TUBE HCG IMMUNOASSAY HCG?

COATED TUBE HCG IMMUNOASSAY HCG is a medical device that received FDA 510(k) clearance on 1984-05-01. The listed applicant is Ventrex Laboratories, Inc.. The 510(k) number is K841023.

When did COATED TUBE HCG IMMUNOASSAY HCG receive FDA 510(k) clearance?

COATED TUBE HCG IMMUNOASSAY HCG received FDA 510(k) clearance on 1984-05-01, under 510(k) number K841023.

Who is the listed applicant for COATED TUBE HCG IMMUNOASSAY HCG?

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

What is the FDA product code for COATED TUBE HCG IMMUNOASSAY HCG?

The FDA product code for COATED TUBE HCG IMMUNOASSAY HCG is JHI.

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Other records listing Ventrex Laboratories, 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.

K914554SPECIFIC IGE EIA-TURBO ASSAYK913833VENTREX ALLERGEN DISCK913434VENTREX COATED TUBE INTACT PTHK905612VENTREX COATED TUBE IGE RADIOIMMUNOASSAYK905636VENTREX COATED TUBE IGE ENZYME IMMUNOASSAYK905247SHBG IRMA KIT

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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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