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FDA 510(k)

TOYO JOZO G-GTP TEST

K-Number: K842104 · 1984-08-10

ApplicantAdvocacy International, Ltd.
Decision Date1984-08-10
Product CodeJPZ
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

TOYO JOZO G-GTP TEST is the device name listed in this FDA 510(k) record. The listed applicant is Advocacy International, Ltd.. It received FDA 510(k) clearance on 1984-08-10 under 510(k) number K842104. The device is classified under product code JPZ. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TOYO JOZO G-GTP TEST?

TOYO JOZO G-GTP TEST is a medical device that received FDA 510(k) clearance on 1984-08-10. The listed applicant is Advocacy International, Ltd.. The 510(k) number is K842104.

When did TOYO JOZO G-GTP TEST receive FDA 510(k) clearance?

TOYO JOZO G-GTP TEST received FDA 510(k) clearance on 1984-08-10, under 510(k) number K842104.

Who is the listed applicant for TOYO JOZO G-GTP TEST?

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

What is the FDA product code for TOYO JOZO G-GTP TEST?

The FDA product code for TOYO JOZO G-GTP TEST is JPZ.

Other records listing Advocacy International, Ltd. 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.

K874027LIPASE UV [TOYO]K873792SEPACELL R-500 AND SEPACELL R-500AK855251MODIFICATION ASAHI NEW PAN-SERIES HEMOFILTERSK855212ASAHI AM SERIES DIALYZERSK854259SEPACELL R-500 & SEPACELL R-500AK842103TOYO JOZO URIC ACID TEST

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Related Devices (Code: JPZ)

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.

K020486CARESIDE GGTCareside, Inc.K961919DMA GAMMA GLUTAMYLTRANSFERASE (GGT) PROCEDUREData Medical Associates, Inc.K923509GAMMA-GTRandox Laboratories, Ltd.K923091KING DIAGNOSTICS GAMMA GT REAGENTKing Diagnostics, Inc.K905618GGT REAGENTAmresco, Inc.K903304ROCHE COBAS READY GGT REAGENTRoche Diagnostic Systems, Inc.

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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