PENTAX Medical Video Colonoscope (EC38-i20cWL)
K-Number: K242110 · 2025-01-03
Device Summary
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
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.