FDA 510(k)

V-PRO maX 2 Low Temperature Sterilization System, V-PRO maX Low Temperature Sterilization System

Numéro K : K222093 · 2022-09-09

DemandeurSteris

Date de décision2022-09-09

Code produitMLR

Comité consultatifHO

DécisionSubstantially Equivalent

Résumé du dispositif

V-PRO maX 2 Low Temperature Sterilization System, V-PRO maX Low Temperature Sterilization System is the device name listed in this FDA 510(k) record. The listed applicant is Steris. It received FDA 510(k) clearance on 2022-09-09 under 510(k) number K222093. The device is classified under product code MLR. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Questions fréquentes

What is the V-PRO maX 2 Low Temperature Sterilization System, V-PRO maX Low Temperature Sterilization System?

V-PRO maX 2 Low Temperature Sterilization System, V-PRO maX Low Temperature Sterilization System is a medical device that received FDA 510(k) clearance on 2022-09-09. The listed applicant is Steris. The 510(k) number is K222093.

When did V-PRO maX 2 Low Temperature Sterilization System, V-PRO maX Low Temperature Sterilization System receive FDA 510(k) clearance?

V-PRO maX 2 Low Temperature Sterilization System, V-PRO maX Low Temperature Sterilization System received FDA 510(k) clearance on 2022-09-09, under 510(k) number K222093.

Who is the listed applicant for V-PRO maX 2 Low Temperature Sterilization System, V-PRO maX Low Temperature Sterilization System?

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

What is the FDA product code for V-PRO maX 2 Low Temperature Sterilization System, V-PRO maX Low Temperature Sterilization System?

The FDA product code for V-PRO maX 2 Low Temperature Sterilization System, V-PRO maX Low Temperature Sterilization System is MLR.

Essais cliniques associés

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Dispositifs connexes (Code : MLR)

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Source officielle

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