Pentax Medical Video Duodenoscope ED32-i10
K-Number: K202365 · 2021-04-01
Device Summary
Frequently Asked Questions
What is the Pentax Medical Video Duodenoscope ED32-i10?
Pentax Medical Video Duodenoscope ED32-i10 is a medical device that received FDA 510(k) clearance on 2021-04-01. It is manufactured by Pentax of America, Inc.. The 510(k) number is K202365.
When was Pentax Medical Video Duodenoscope ED32-i10 approved by the FDA?
Pentax Medical Video Duodenoscope ED32-i10 received FDA 510(k) clearance on 2021-04-01, under approval number K202365.
What company makes Pentax Medical Video Duodenoscope ED32-i10?
Pentax Medical Video Duodenoscope ED32-i10 is manufactured by Pentax of America, Inc..
What is the FDA product code for Pentax Medical Video Duodenoscope ED32-i10?
The FDA product code for Pentax Medical Video Duodenoscope ED32-i10 is FDT.
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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.