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FDA 510(k)

CAP PLUS

K-Number: K063050 · 2007-11-19

ApplicantEtex Corp.
Decision Date2007-11-19
Product CodeMQV
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

CAP PLUS is the device name listed in this FDA 510(k) record. The listed applicant is Etex Corp.. It received FDA 510(k) clearance on 2007-11-19 under 510(k) number K063050. The device is classified under product code MQV. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CAP PLUS?

CAP PLUS is a medical device that received FDA 510(k) clearance on 2007-11-19. The listed applicant is Etex Corp.. The 510(k) number is K063050.

When did CAP PLUS receive FDA 510(k) clearance?

CAP PLUS received FDA 510(k) clearance on 2007-11-19, under 510(k) number K063050.

Who is the listed applicant for CAP PLUS?

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

What is the FDA product code for CAP PLUS?

The FDA product code for CAP PLUS is MQV.

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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.

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