EndoGator Endoscopy Irrigation Tubing
K-Number: K220395 · 2022-03-11
Device Summary
Frequently Asked Questions
What is the EndoGator Endoscopy Irrigation Tubing?
EndoGator Endoscopy Irrigation Tubing is a medical device that received FDA 510(k) clearance on 2022-03-11. The listed applicant is STERIS Corporation. The 510(k) number is K220395.
When did EndoGator Endoscopy Irrigation Tubing receive FDA 510(k) clearance?
EndoGator Endoscopy Irrigation Tubing received FDA 510(k) clearance on 2022-03-11, under 510(k) number K220395.
Who is the listed applicant for EndoGator Endoscopy Irrigation Tubing?
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 EndoGator Endoscopy Irrigation Tubing?
The FDA product code for EndoGator Endoscopy Irrigation Tubing is FEQ.
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: FEQ)
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.