FDA 510(k)

AMSCO V-PRO 1 AND V-PRO 1 PLUS LOW TEMPERATURE STERILIZATION UNITS

K-Number: K111810 · 2011-09-02

Decision Date2011-09-02

Product CodeMLR

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

AMSCO V-PRO 1 AND V-PRO 1 PLUS LOW TEMPERATURE STERILIZATION UNITS is the device name listed in this FDA 510(k) record. The listed applicant is STERIS Corporation. It received FDA 510(k) clearance on 2011-09-02 under 510(k) number K111810. The device is classified under product code MLR. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AMSCO V-PRO 1 AND V-PRO 1 PLUS LOW TEMPERATURE STERILIZATION UNITS?

AMSCO V-PRO 1 AND V-PRO 1 PLUS LOW TEMPERATURE STERILIZATION UNITS is a medical device that received FDA 510(k) clearance on 2011-09-02. The listed applicant is STERIS Corporation. The 510(k) number is K111810.

When did AMSCO V-PRO 1 AND V-PRO 1 PLUS LOW TEMPERATURE STERILIZATION UNITS receive FDA 510(k) clearance?

AMSCO V-PRO 1 AND V-PRO 1 PLUS LOW TEMPERATURE STERILIZATION UNITS received FDA 510(k) clearance on 2011-09-02, under 510(k) number K111810.

Who is the listed applicant for AMSCO V-PRO 1 AND V-PRO 1 PLUS LOW TEMPERATURE STERILIZATION UNITS?

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

What is the FDA product code for AMSCO V-PRO 1 AND V-PRO 1 PLUS LOW TEMPERATURE STERILIZATION UNITS?

The FDA product code for AMSCO V-PRO 1 AND V-PRO 1 PLUS LOW TEMPERATURE STERILIZATION UNITS is MLR.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.