FDA 510(k)

CAVROPUMP

K-Number: K871129 · 1987-08-28

Decision Date1987-08-28

Product CodeDXT

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

CAVROPUMP is the device name listed in this FDA 510(k) record. The listed applicant is Life-Tech Intl., Inc.. It received FDA 510(k) clearance on 1987-08-28 under 510(k) number K871129. The device is classified under product code DXT. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CAVROPUMP?

CAVROPUMP is a medical device that received FDA 510(k) clearance on 1987-08-28. The listed applicant is Life-Tech Intl., Inc.. The 510(k) number is K871129.

When did CAVROPUMP receive FDA 510(k) clearance?

CAVROPUMP received FDA 510(k) clearance on 1987-08-28, under 510(k) number K871129.

Who is the listed applicant for CAVROPUMP?

The FDA 510(k) record lists Life-Tech Intl., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CAVROPUMP?

The FDA product code for CAVROPUMP is DXT.

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Other records listing Life-Tech Intl., Inc. as applicant

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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.