FDA 510(k)

PONCEAU S STAIN SET

K-Number: K792550 · 1980-01-16

ApplicantElectrophoresis Corp. of America

Decision Date1980-01-16

Product CodeKQC

Advisory CommitteeHE

DecisionSubstantially Equivalent

Device Summary

PONCEAU S STAIN SET 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 1980-01-16 under 510(k) number K792550. The device is classified under product code KQC. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PONCEAU S STAIN SET?

PONCEAU S STAIN SET is a medical device that received FDA 510(k) clearance on 1980-01-16. The listed applicant is Electrophoresis Corp. of America. The 510(k) number is K792550.

When did PONCEAU S STAIN SET receive FDA 510(k) clearance?

PONCEAU S STAIN SET received FDA 510(k) clearance on 1980-01-16, under 510(k) number K792550.

Who is the listed applicant for PONCEAU S STAIN SET?

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 PONCEAU S STAIN SET?

The FDA product code for PONCEAU S STAIN SET is KQC.

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Other records listing Electrophoresis Corp. of America as applicant

K802396GENERAL PROCEDURE AGAROSE FILM K792548ALKALINE PHOSPHATASE MARKER K792553AGAROSE BARBITAL-EDTA BUFFER K792551ALKALINE PHOSPHATASE REAGENT K792547AGAROSE BARBITAL BUFFER K792574MOPSO BUFFER

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Related Devices (Code: KQC)

K882873FIELDTEX HEMATOXYLINAnatech, Ltd.K852843GENERAL DIAGNOSTICS COAG-A-MATE XCWarner-Lambert Co.K843619RETIC-SETR&D Systems, Inc.K841848RETIC-SETR&D Systems, Inc.K792496VOLU-SOL NMB RETICULOCYTE STAINVolu Sol Medical Industries K791007STAT DIFF STAINBioscientific

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.