PENTAX Medical Video Duedenoscope ED34-i10T2
K-Number: K210710 · 2021-04-09
Device Summary
Frequently Asked Questions
What is the PENTAX Medical Video Duedenoscope ED34-i10T2?
PENTAX Medical Video Duedenoscope ED34-i10T2 is a medical device that received FDA 510(k) clearance on 2021-04-09. It is manufactured by Pentax of America, Inc.. The 510(k) number is K210710.
When was PENTAX Medical Video Duedenoscope ED34-i10T2 approved by the FDA?
PENTAX Medical Video Duedenoscope ED34-i10T2 received FDA 510(k) clearance on 2021-04-09, under approval number K210710.
What company makes PENTAX Medical Video Duedenoscope ED34-i10T2?
PENTAX Medical Video Duedenoscope ED34-i10T2 is manufactured by Pentax of America, Inc..
What is the FDA product code for PENTAX Medical Video Duedenoscope ED34-i10T2?
The FDA product code for PENTAX Medical Video Duedenoscope ED34-i10T2 is FDT.
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Related PubMed Literature
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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.