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FDA 510(k)

AMSCO WARMING CABINET

K-Number: K111870 · 2011-07-29

ApplicantSTERIS Corporation
Decision Date2011-07-29
Product CodeLGZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

AMSCO WARMING CABINET is the device name listed in this FDA 510(k) record. The listed applicant is STERIS Corporation. It received FDA 510(k) clearance on 2011-07-29 under 510(k) number K111870. The device is classified under product code LGZ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AMSCO WARMING CABINET?

AMSCO WARMING CABINET is a medical device that received FDA 510(k) clearance on 2011-07-29. The listed applicant is STERIS Corporation. The 510(k) number is K111870.

When did AMSCO WARMING CABINET receive FDA 510(k) clearance?

AMSCO WARMING CABINET received FDA 510(k) clearance on 2011-07-29, under 510(k) number K111870.

Who is the listed applicant for AMSCO WARMING CABINET?

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 WARMING CABINET?

The FDA product code for AMSCO WARMING CABINET is LGZ.

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Related Devices (Code: LGZ)

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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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