ArgoCap (200.52)
K-Number: K242586 · 2025-05-22
ApplicantOvesco Endoscopy AG
Decision Date2025-05-22
Product CodeOCX
Advisory CommitteeGU
DecisionSubstantially Equivalent
Device Summary
ArgoCap (200.52) is a medical device manufactured by Ovesco Endoscopy AG. It received FDA 510(k) clearance on 2025-05-22 under approval number K242586. The device is classified under product code OCX. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the ArgoCap (200.52)?
ArgoCap (200.52) is a medical device that received FDA 510(k) clearance on 2025-05-22. It is manufactured by Ovesco Endoscopy AG. The 510(k) number is K242586.
When was ArgoCap (200.52) approved by the FDA?
ArgoCap (200.52) received FDA 510(k) clearance on 2025-05-22, under approval number K242586.
What company makes ArgoCap (200.52)?
ArgoCap (200.52) is manufactured by Ovesco Endoscopy AG.
What is the FDA product code for ArgoCap (200.52)?
The FDA product code for ArgoCap (200.52) is OCX.
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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.