FDA 510(k)

MOLLRING MULTITASC

K-Number: K121415 · 2012-09-05

Decision Date2012-09-05

Product CodeDWX

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

MOLLRING MULTITASC is the device name listed in this FDA 510(k) record. The listed applicant is LeMaitre Vascular, Inc.. It received FDA 510(k) clearance on 2012-09-05 under 510(k) number K121415. The device is classified under product code DWX. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MOLLRING MULTITASC?

MOLLRING MULTITASC is a medical device that received FDA 510(k) clearance on 2012-09-05. The listed applicant is LeMaitre Vascular, Inc.. The 510(k) number is K121415.

When did MOLLRING MULTITASC receive FDA 510(k) clearance?

MOLLRING MULTITASC received FDA 510(k) clearance on 2012-09-05, under 510(k) number K121415.

Who is the listed applicant for MOLLRING MULTITASC?

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

What is the FDA product code for MOLLRING MULTITASC?

The FDA product code for MOLLRING MULTITASC is DWX.

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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.