CELERITY 20 Steam Incubator
K-Number: K173670 · 2018-02-12
Device Summary
Frequently Asked Questions
What is the CELERITY 20 Steam Incubator?
CELERITY 20 Steam Incubator is a medical device that received FDA 510(k) clearance on 2018-02-12. The listed applicant is STERIS Corporation. The 510(k) number is K173670.
When did CELERITY 20 Steam Incubator receive FDA 510(k) clearance?
CELERITY 20 Steam Incubator received FDA 510(k) clearance on 2018-02-12, under 510(k) number K173670.
Who is the listed applicant for CELERITY 20 Steam Incubator?
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 CELERITY 20 Steam Incubator?
The FDA product code for CELERITY 20 Steam Incubator is FRC.
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: FRC)
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.