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FDA 510(k)

AMSCO V-PRO

K-Number: K112813 · 2011-12-01

ApplicantSteris Corp
Decision Date2011-12-01
Product CodeMLR
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

AMSCO V-PRO is the device name listed in this FDA 510(k) record. The listed applicant is Steris Corp. It received FDA 510(k) clearance on 2011-12-01 under 510(k) number K112813. 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?

AMSCO V-PRO is a medical device that received FDA 510(k) clearance on 2011-12-01. The listed applicant is Steris Corp. The 510(k) number is K112813.

When did AMSCO V-PRO receive FDA 510(k) clearance?

AMSCO V-PRO received FDA 510(k) clearance on 2011-12-01, under 510(k) number K112813.

Who is the listed applicant for AMSCO V-PRO?

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

What is the FDA product code for AMSCO V-PRO?

The FDA product code for AMSCO V-PRO is MLR.

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Related Devices (Code: MLR)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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.

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