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FDA 510(k)

VENTREZYME BETA-HCG IMMUNOASSAY HCG

K-Number: K841081 · 1984-05-07

Decision Date1984-05-07
Product CodeJHI
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

VENTREZYME BETA-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 1984-05-07 under 510(k) number K841081. 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 VENTREZYME BETA-HCG IMMUNOASSAY HCG?

VENTREZYME BETA-HCG IMMUNOASSAY HCG is a medical device that received FDA 510(k) clearance on 1984-05-07. The listed applicant is Ventrex Laboratories, Inc.. The 510(k) number is K841081.

When did VENTREZYME BETA-HCG IMMUNOASSAY HCG receive FDA 510(k) clearance?

VENTREZYME BETA-HCG IMMUNOASSAY HCG received FDA 510(k) clearance on 1984-05-07, under 510(k) number K841081.

Who is the listed applicant for VENTREZYME BETA-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 VENTREZYME BETA-HCG IMMUNOASSAY HCG?

The FDA product code for VENTREZYME BETA-HCG IMMUNOASSAY HCG 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 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.

View all 82 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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