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FDA 510(k)

SPECIAL PROCEDURE AQAROSE FILM

K-Number: K802395 · 1980-11-26

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

Device Summary

SPECIAL PROCEDURE AQAROSE FILM is the device name listed in this FDA 510(k) record. The listed applicant is Electrophoresis Corp.. It received FDA 510(k) clearance on 1980-11-26 under 510(k) number K802395. 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 SPECIAL PROCEDURE AQAROSE FILM?

SPECIAL PROCEDURE AQAROSE FILM is a medical device that received FDA 510(k) clearance on 1980-11-26. The listed applicant is Electrophoresis Corp.. The 510(k) number is K802395.

When did SPECIAL PROCEDURE AQAROSE FILM receive FDA 510(k) clearance?

SPECIAL PROCEDURE AQAROSE FILM received FDA 510(k) clearance on 1980-11-26, under 510(k) number K802395.

Who is the listed applicant for SPECIAL PROCEDURE AQAROSE FILM?

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

What is the FDA product code for SPECIAL PROCEDURE AQAROSE FILM?

The FDA product code for SPECIAL PROCEDURE AQAROSE FILM is JJN.

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Other records listing Electrophoresis Corp. 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.

K790309CPK ISOENZYME SUBSTRATEK790310HEMOGLOBIN CONTROLSK790311LDH ISOENZYME REAGENT

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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