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FDA 510(k)

ROCHE(R) B-HCG RIA URINE STANDARD

K-Number: K820942 · 1982-05-03

ApplicantHoffmann-La Roche, Inc.
Decision Date1982-05-03
Product CodeJHI
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

ROCHE(R) B-HCG RIA URINE STANDARD is the device name listed in this FDA 510(k) record. The listed applicant is Hoffmann-La Roche, Inc.. It received FDA 510(k) clearance on 1982-05-03 under 510(k) number K820942. 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 ROCHE(R) B-HCG RIA URINE STANDARD?

ROCHE(R) B-HCG RIA URINE STANDARD is a medical device that received FDA 510(k) clearance on 1982-05-03. The listed applicant is Hoffmann-La Roche, Inc.. The 510(k) number is K820942.

When did ROCHE(R) B-HCG RIA URINE STANDARD receive FDA 510(k) clearance?

ROCHE(R) B-HCG RIA URINE STANDARD received FDA 510(k) clearance on 1982-05-03, under 510(k) number K820942.

Who is the listed applicant for ROCHE(R) B-HCG RIA URINE STANDARD?

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

What is the FDA product code for ROCHE(R) B-HCG RIA URINE STANDARD?

The FDA product code for ROCHE(R) B-HCG RIA URINE STANDARD is JHI.

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Other records listing Hoffmann-La Roche, 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.

K850727BHCG-ROCHE EIAK831694RENAKK830480ABUSCREEN RADIOIMMUNOASSAY-COCAINE METAK830462ABUSCREEN RADIOUMMUNOASSAY--URINEK830482ABUSCREEN RADIOIMMUNOASSAY-AMPHETAMINEK830461ABUSCREEN RADIOUMMUNOASSAY-METHAQUALONE

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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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