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FDA 510(k)

PENTAX Medical Video Colonoscope (EC38-i20cWL)

K-Number: K242110 · 2025-01-03

Decision Date2025-01-03
Product CodeFDF
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

PENTAX Medical Video Colonoscope (EC38-i20cWL) is a medical device manufactured by Pentax of America, Inc.. It received FDA 510(k) clearance on 2025-01-03 under approval number K242110. The device is classified under product code FDF. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PENTAX Medical Video Colonoscope (EC38-i20cWL)?

PENTAX Medical Video Colonoscope (EC38-i20cWL) is a medical device that received FDA 510(k) clearance on 2025-01-03. It is manufactured by Pentax of America, Inc.. The 510(k) number is K242110.

When was PENTAX Medical Video Colonoscope (EC38-i20cWL) approved by the FDA?

PENTAX Medical Video Colonoscope (EC38-i20cWL) received FDA 510(k) clearance on 2025-01-03, under approval number K242110.

What company makes PENTAX Medical Video Colonoscope (EC38-i20cWL)?

PENTAX Medical Video Colonoscope (EC38-i20cWL) is manufactured by Pentax of America, Inc..

What is the FDA product code for PENTAX Medical Video Colonoscope (EC38-i20cWL)?

The FDA product code for PENTAX Medical Video Colonoscope (EC38-i20cWL) is FDF.

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Official Source

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