FDA 510(k)

CLEARING SOLUTION #ECA01976

K-Number: K781898 · 1978-12-20

ApplicantElectrophoresis Corp. of America

Decision Date1978-12-20

Product CodeJQK

Advisory CommitteeCH

DecisionSubstantially Equivalent

Device Summary

CLEARING SOLUTION #ECA01976 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 1978-12-20 under 510(k) number K781898. The device is classified under product code JQK. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CLEARING SOLUTION #ECA01976?

CLEARING SOLUTION #ECA01976 is a medical device that received FDA 510(k) clearance on 1978-12-20. The listed applicant is Electrophoresis Corp. of America. The 510(k) number is K781898.

When did CLEARING SOLUTION #ECA01976 receive FDA 510(k) clearance?

CLEARING SOLUTION #ECA01976 received FDA 510(k) clearance on 1978-12-20, under 510(k) number K781898.

Who is the listed applicant for CLEARING SOLUTION #ECA01976?

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 CLEARING SOLUTION #ECA01976?

The FDA product code for CLEARING SOLUTION #ECA01976 is JQK.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.