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FDA 510(k)

ALKALINE PHOSPHATASE REAGENT

K-Number: K792551 · 1980-01-29

ApplicantElectrophoresis Corp. of America
Decision Date1980-01-29
Product CodeCJH
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

ALKALINE PHOSPHATASE REAGENT is the device name listed in this FDA 510(k) record. The listed applicant is Electrophoresis Corp. of America. It received FDA 510(k) clearance on 1980-01-29 under 510(k) number K792551. The device is classified under product code CJH. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ALKALINE PHOSPHATASE REAGENT?

ALKALINE PHOSPHATASE REAGENT is a medical device that received FDA 510(k) clearance on 1980-01-29. The listed applicant is Electrophoresis Corp. of America. The 510(k) number is K792551.

When did ALKALINE PHOSPHATASE REAGENT receive FDA 510(k) clearance?

ALKALINE PHOSPHATASE REAGENT received FDA 510(k) clearance on 1980-01-29, under 510(k) number K792551.

Who is the listed applicant for ALKALINE PHOSPHATASE REAGENT?

The FDA 510(k) record lists Electrophoresis Corp. of America as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ALKALINE PHOSPHATASE REAGENT?

The FDA product code for ALKALINE PHOSPHATASE REAGENT is CJH.

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Other records listing Electrophoresis Corp. of America 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.

K802396GENERAL PROCEDURE AGAROSE FILMK792553AGAROSE BARBITAL-EDTA BUFFERK792548ALKALINE PHOSPHATASE MARKERK792547AGAROSE BARBITAL BUFFERK792574MOPSO BUFFERK792550PONCEAU S STAIN SET

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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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