FDA 510(k)

AGAROSE BARBITAL BUFFER

K-Number: K792547 · 1980-01-29

ApplicantElectrophoresis Corp. of America

Decision Date1980-01-29

Product CodeJJN

Advisory CommitteeCH

DecisionSubstantially Equivalent

Device Summary

AGAROSE BARBITAL BUFFER 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 K792547. 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 AGAROSE BARBITAL BUFFER?

AGAROSE BARBITAL BUFFER 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 K792547.

When did AGAROSE BARBITAL BUFFER receive FDA 510(k) clearance?

AGAROSE BARBITAL BUFFER received FDA 510(k) clearance on 1980-01-29, under 510(k) number K792547.

Who is the listed applicant for AGAROSE BARBITAL BUFFER?

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 AGAROSE BARBITAL BUFFER?

The FDA product code for AGAROSE BARBITAL BUFFER is JJN.

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Other records listing Electrophoresis Corp. of America as applicant

K802396GENERAL PROCEDURE AGAROSE FILM K792553AGAROSE BARBITAL-EDTA BUFFER K792548ALKALINE PHOSPHATASE MARKER K792551ALKALINE PHOSPHATASE REAGENT K792574MOPSO BUFFER K792550PONCEAU S STAIN SET

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Related Devices (Code: JJN)

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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.