Reliance EPS Endoscope Processing System and Reliance DG Dry Germicide
K-Number: K220361 · 2022-03-10
Device Summary
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. The listed applicant is STERIS Corporation. The 510(k) number is K220361.
When did Reliance EPS Endoscope Processing System and Reliance DG Dry Germicide receive FDA 510(k) clearance?
Reliance EPS Endoscope Processing System and Reliance DG Dry Germicide received FDA 510(k) clearance on 2022-03-10, under 510(k) number K220361.
Who is the listed applicant for Reliance EPS Endoscope Processing System and Reliance DG Dry Germicide?
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 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.
Other records listing STERIS Corporation as applicant
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.
Related Devices (Code: NZA)
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.
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.