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FDA 510(k)

Reliance Endoscope Processing System

K-Number: K200989 · 2020-05-14

ApplicantSTERIS Corporation
Decision Date2020-05-14
Product CodeNZA
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

Reliance Endoscope Processing System is a medical device manufactured by STERIS Corporation. It received FDA 510(k) clearance on 2020-05-14 under approval number K200989. 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 2020-05-14. It is manufactured by STERIS Corporation. The 510(k) number is K200989.

When was Reliance Endoscope Processing System approved by the FDA?

Reliance Endoscope Processing System received FDA 510(k) clearance on 2020-05-14, under approval number K200989.

What company makes Reliance Endoscope Processing System?

Reliance Endoscope Processing System is manufactured by STERIS Corporation.

What is the FDA product code for Reliance Endoscope Processing System?

The FDA product code for Reliance Endoscope Processing System is NZA.

Related Clinical Trials

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Related PubMed Literature

PMID: 42056377 Signal detection of adverse events in medical devices using natural language processing: a case study in pelvic mesh. Scientific reports (2026)

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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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