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FDA 510(k)

Reliance EPS Endoscope Processing System and Reliance DG Dry Germicide

K-Number: K220361 · 2022-03-10

ApplicantSTERIS Corporation
Decision Date2022-03-10
Product CodeNZA
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

Reliance EPS Endoscope Processing System and Reliance DG Dry Germicide is a medical device manufactured by STERIS Corporation. It received FDA 510(k) clearance on 2022-03-10 under approval number K220361. 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 EPS Endoscope Processing System and Reliance DG Dry Germicide?

Reliance EPS Endoscope Processing System and Reliance DG Dry Germicide is a medical device that received FDA 510(k) clearance on 2022-03-10. It is manufactured by STERIS Corporation. The 510(k) number is K220361.

When was Reliance EPS Endoscope Processing System and Reliance DG Dry Germicide approved by the FDA?

Reliance EPS Endoscope Processing System and Reliance DG Dry Germicide received FDA 510(k) clearance on 2022-03-10, under approval number K220361.

What company makes Reliance EPS Endoscope Processing System and Reliance DG Dry Germicide?

Reliance EPS Endoscope Processing System and Reliance DG Dry Germicide is manufactured by STERIS Corporation.

What is the FDA product code for Reliance EPS Endoscope Processing System and Reliance DG Dry Germicide?

The FDA product code for Reliance EPS Endoscope Processing System and Reliance DG Dry Germicide is NZA.

Related Clinical Trials

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Related PubMed Literature

PMID: 38493931 Establishing finite element model credibility of a pedicle screw system under compression-bending: An end-to-end example of the ASME V&V 40 standard. Methods (San Diego, Calif.) (2024) PMID: 29653650 Comparison of adverse event and device problem rates for transcatheter aortic valve replacement and Mitraclip procedures as reported by the Transcatheter Valve Therapy Registry and the Food and Drug Administration postmarket surveillance data. American heart journal (2018)

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Related Devices (Code: NZA)

K200989Reliance Endoscope Processing SystemSTERIS Corporation K203223Reliance EPS Endoscope Processing System and Reliance DG Dry GermicideSteris K232918enspire 300 Series Automated Endoscope ReprocessorSTERIS Corporation K230560enspire 300 Series Automated Endoscope Reprocessor SystemSTERIS Corporation

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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