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FDA 510(k)

Recovery Cone Removal System

K-Number: K152136 · 2016-02-18

ApplicantC.R. Bard, Inc.
Decision Date2016-02-18
Product CodeMMX
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

Recovery Cone Removal System is a medical device manufactured by C.R. Bard, Inc.. It received FDA 510(k) clearance on 2016-02-18 under approval number K152136. The device is classified under product code MMX. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Recovery Cone Removal System?

Recovery Cone Removal System is a medical device that received FDA 510(k) clearance on 2016-02-18. It is manufactured by C.R. Bard, Inc.. The 510(k) number is K152136.

When was Recovery Cone Removal System approved by the FDA?

Recovery Cone Removal System received FDA 510(k) clearance on 2016-02-18, under approval number K152136.

What company makes Recovery Cone Removal System?

Recovery Cone Removal System is manufactured by C.R. Bard, Inc..

What is the FDA product code for Recovery Cone Removal System?

The FDA product code for Recovery Cone Removal System is MMX.

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Related PubMed Literature

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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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