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FDA 510(k)

GENERAL PROCEDURE AGAROSE FILM

K-Number: K802396 · 1980-11-26

ApplicantElectrophoresis Corp. of America
Decision Date1980-11-26
Product CodeJJN
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

GENERAL PROCEDURE AGAROSE FILM 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 1980-11-26 under 510(k) number K802396. The device is classified under product code JJN. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GENERAL PROCEDURE AGAROSE FILM?

GENERAL PROCEDURE AGAROSE FILM is a medical device that received FDA 510(k) clearance on 1980-11-26. The listed applicant is Electrophoresis Corp. of America. The 510(k) number is K802396.

When did GENERAL PROCEDURE AGAROSE FILM receive FDA 510(k) clearance?

GENERAL PROCEDURE AGAROSE FILM received FDA 510(k) clearance on 1980-11-26, under 510(k) number K802396.

Who is the listed applicant for GENERAL PROCEDURE AGAROSE FILM?

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 GENERAL PROCEDURE AGAROSE FILM?

The FDA product code for GENERAL PROCEDURE AGAROSE FILM is JJN.

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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.

K792548ALKALINE PHOSPHATASE MARKERK792553AGAROSE BARBITAL-EDTA BUFFERK792551ALKALINE PHOSPHATASE REAGENTK792547AGAROSE BARBITAL BUFFERK792574MOPSO BUFFERK792550PONCEAU S STAIN SET

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Related Devices (Code: JJN)

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.

K924021POWER SUPPLYThe Binding Site, Ltd.K924020ELECTROPHORESIS TANKThe Binding Site, Ltd.K882344ELECTR-TRANSBLOTTERThe W.E.P. Co.K881852REP SP ELECTROPHORESIS SYSTEM CAT NO. 3170Helena LaboratoriesK882163HELENA REP GEL PROCESSORHelena LaboratoriesK873352RAPID ELECTROPHORESIS SYSTEM (REP)Helena Laboratories

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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