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FDA 510(k)

LIPOPROTEIN STAIN

K-Number: K781122 · 1978-08-31

ApplicantElectrophoresis Corp. of America
Decision Date1978-08-31
Product CodeHZG
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

LIPOPROTEIN STAIN 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 1978-08-31 under 510(k) number K781122. The device is classified under product code HZG. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LIPOPROTEIN STAIN?

LIPOPROTEIN STAIN is a medical device that received FDA 510(k) clearance on 1978-08-31. The listed applicant is Electrophoresis Corp. of America. The 510(k) number is K781122.

When did LIPOPROTEIN STAIN receive FDA 510(k) clearance?

LIPOPROTEIN STAIN received FDA 510(k) clearance on 1978-08-31, under 510(k) number K781122.

Who is the listed applicant for LIPOPROTEIN STAIN?

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 LIPOPROTEIN STAIN?

The FDA product code for LIPOPROTEIN STAIN is HZG.

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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 FILMK792548ALKALINE PHOSPHATASE MARKERK792553AGAROSE BARBITAL-EDTA BUFFERK792551ALKALINE PHOSPHATASE REAGENTK792547AGAROSE BARBITAL BUFFERK792574MOPSO BUFFER

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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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