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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 the device name listed in this FDA 510(k) record. The listed applicant is C.R. Bard, Inc.. It received FDA 510(k) clearance on 2016-02-18 under 510(k) 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. The listed applicant is C.R. Bard, Inc.. The 510(k) number is K152136.

When did Recovery Cone Removal System receive FDA 510(k) clearance?

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

Who is the listed applicant for Recovery Cone Removal System?

The FDA 510(k) record lists C.R. Bard, Inc. as the applicant. This does not by itself establish the device manufacturer.

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 Devices (Code: MMX)

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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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