FDA 510(k)

ECA BUFFER PH 8.8

K-Number: K781118 · 1978-08-10

ApplicantElectrophoresis Corp. of America

Decision Date1978-08-10

Product CodeCEF

Advisory CommitteeCH

DecisionSubstantially Equivalent

Device Summary

ECA BUFFER PH 8.8 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 K781118. 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 ECA BUFFER PH 8.8?

ECA BUFFER PH 8.8 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 K781118.

When did ECA BUFFER PH 8.8 receive FDA 510(k) clearance?

ECA BUFFER PH 8.8 received FDA 510(k) clearance on 1978-08-10, under 510(k) number K781118.

Who is the listed applicant for ECA BUFFER PH 8.8?

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 ECA BUFFER PH 8.8?

The FDA product code for ECA BUFFER PH 8.8 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.