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FDA 510(k)

PENTAX Medical Video Duedenoscope ED34-i10T2

K-Number: K210710 · 2021-04-09

Decision Date2021-04-09
Product CodeFDT
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

PENTAX Medical Video Duedenoscope ED34-i10T2 is a medical device manufactured by Pentax of America, Inc.. It received FDA 510(k) clearance on 2021-04-09 under approval number K210710. The device is classified under product code FDT. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

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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Official Source

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