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FDA 510(k)

CAREVENT

K-Number: K062240 · 2006-10-16

ApplicantChief Medical, LLC
Decision Date2006-10-16
Product CodeKNY
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

CAREVENT is the device name listed in this FDA 510(k) record. The listed applicant is Chief Medical, LLC. It received FDA 510(k) clearance on 2006-10-16 under 510(k) number K062240. The device is classified under product code KNY. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CAREVENT?

CAREVENT is a medical device that received FDA 510(k) clearance on 2006-10-16. The listed applicant is Chief Medical, LLC. The 510(k) number is K062240.

When did CAREVENT receive FDA 510(k) clearance?

CAREVENT received FDA 510(k) clearance on 2006-10-16, under 510(k) number K062240.

Who is the listed applicant for CAREVENT?

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

What is the FDA product code for CAREVENT?

The FDA product code for CAREVENT is KNY.

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Related Devices (Code: KNY)

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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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