FDA 510(k)

Single-Loop Snare Retrieval Kit, Triple-Loop Snare Retrieval Kit

Numéro K : K232443 · 2023-09-07

Date de décision2023-09-07

Code produitMMX

Comité consultatifCV

DécisionSubstantially Equivalent

Résumé du dispositif

Single-Loop Snare Retrieval Kit, Triple-Loop Snare Retrieval Kit is the device name listed in this FDA 510(k) record. The listed applicant is Argon Medical Devices, Inc.. It received FDA 510(k) clearance on 2023-09-07 under 510(k) number K232443. The device is classified under product code MMX. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Questions fréquentes

What is the Single-Loop Snare Retrieval Kit, Triple-Loop Snare Retrieval Kit?

Single-Loop Snare Retrieval Kit, Triple-Loop Snare Retrieval Kit is a medical device that received FDA 510(k) clearance on 2023-09-07. The listed applicant is Argon Medical Devices, Inc.. The 510(k) number is K232443.

When did Single-Loop Snare Retrieval Kit, Triple-Loop Snare Retrieval Kit receive FDA 510(k) clearance?

Single-Loop Snare Retrieval Kit, Triple-Loop Snare Retrieval Kit received FDA 510(k) clearance on 2023-09-07, under 510(k) number K232443.

Who is the listed applicant for Single-Loop Snare Retrieval Kit, Triple-Loop Snare Retrieval Kit?

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

What is the FDA product code for Single-Loop Snare Retrieval Kit, Triple-Loop Snare Retrieval Kit?

The FDA product code for Single-Loop Snare Retrieval Kit, Triple-Loop Snare Retrieval Kit is MMX.

Essais cliniques associés

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Source officielle

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