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FDA 510(k)

CLAMPEASE FA

K-Number: K863427 · 1986-11-20

ApplicantFreund Medical Products
Decision Date1986-11-20
Product CodeDXC
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

CLAMPEASE FA is the device name listed in this FDA 510(k) record. The listed applicant is Freund Medical Products. It received FDA 510(k) clearance on 1986-11-20 under 510(k) number K863427. The device is classified under product code DXC. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CLAMPEASE FA?

CLAMPEASE FA is a medical device that received FDA 510(k) clearance on 1986-11-20. The listed applicant is Freund Medical Products. The 510(k) number is K863427.

When did CLAMPEASE FA receive FDA 510(k) clearance?

CLAMPEASE FA received FDA 510(k) clearance on 1986-11-20, under 510(k) number K863427.

Who is the listed applicant for CLAMPEASE FA?

The FDA 510(k) record lists Freund Medical Products as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CLAMPEASE FA?

The FDA product code for CLAMPEASE FA is DXC.

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Related Devices (Code: DXC)

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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.

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