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FDA 510(k)

RELIANCE ENDOSCOPE PROCESSING SYSTEM

K-Number: K110453 · 2011-03-16

ApplicantSTERIS Corporation
Decision Date2011-03-16
Product CodeNZA
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

RELIANCE ENDOSCOPE PROCESSING 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 2011-03-16 under 510(k) number K110453. The device is classified under product code NZA. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RELIANCE ENDOSCOPE PROCESSING SYSTEM?

RELIANCE ENDOSCOPE PROCESSING SYSTEM is a medical device that received FDA 510(k) clearance on 2011-03-16. The listed applicant is STERIS Corporation. The 510(k) number is K110453.

When did RELIANCE ENDOSCOPE PROCESSING SYSTEM receive FDA 510(k) clearance?

RELIANCE ENDOSCOPE PROCESSING SYSTEM received FDA 510(k) clearance on 2011-03-16, under 510(k) number K110453.

Who is the listed applicant for RELIANCE ENDOSCOPE PROCESSING 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 RELIANCE ENDOSCOPE PROCESSING SYSTEM?

The FDA product code for RELIANCE ENDOSCOPE PROCESSING SYSTEM is NZA.

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Related Devices (Code: NZA)

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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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