FDA 510(k)

TRICHLORACETIC ACID 7.5%

K-Number: K781120 · 1978-08-10

ApplicantElectrophoresis Corp. of America

Decision Date1978-08-10

Product CodeCEF

Advisory CommitteeCH

DecisionSubstantially Equivalent

Device Summary

TRICHLORACETIC ACID 7.5% 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 1978-08-10 under 510(k) number K781120. The device is classified under product code CEF. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TRICHLORACETIC ACID 7.5%?

TRICHLORACETIC ACID 7.5% is a medical device that received FDA 510(k) clearance on 1978-08-10. The listed applicant is Electrophoresis Corp. of America. The 510(k) number is K781120.

When did TRICHLORACETIC ACID 7.5% receive FDA 510(k) clearance?

TRICHLORACETIC ACID 7.5% received FDA 510(k) clearance on 1978-08-10, under 510(k) number K781120.

Who is the listed applicant for TRICHLORACETIC ACID 7.5%?

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 TRICHLORACETIC ACID 7.5%?

The FDA product code for TRICHLORACETIC ACID 7.5% is CEF.

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Other records listing Electrophoresis Corp. of America as applicant

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Related Devices (Code: CEF)

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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.