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FDA 510(k)

AMSCO V-PRO MAX LOW TEMPERATURE STERILIZATION SYSTEM

K-Number: K112760 · 2011-11-22

ApplicantSTERIS Corporation
Decision Date2011-11-22
Product CodeMLR
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

AMSCO V-PRO MAX LOW TEMPERATURE STERILIZATION SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is STERIS Corporation. It received FDA 510(k) clearance on 2011-11-22 under 510(k) number K112760. 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 MAX LOW TEMPERATURE STERILIZATION SYSTEM?

AMSCO V-PRO MAX LOW TEMPERATURE STERILIZATION SYSTEM is a medical device that received FDA 510(k) clearance on 2011-11-22. The listed applicant is STERIS Corporation. The 510(k) number is K112760.

When did AMSCO V-PRO MAX LOW TEMPERATURE STERILIZATION SYSTEM receive FDA 510(k) clearance?

AMSCO V-PRO MAX LOW TEMPERATURE STERILIZATION SYSTEM received FDA 510(k) clearance on 2011-11-22, under 510(k) number K112760.

Who is the listed applicant for AMSCO V-PRO MAX LOW TEMPERATURE STERILIZATION SYSTEM?

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 MAX LOW TEMPERATURE STERILIZATION SYSTEM?

The FDA product code for AMSCO V-PRO MAX LOW TEMPERATURE STERILIZATION SYSTEM is MLR.

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Related Devices (Code: MLR)

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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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