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FDA 510(k)

BARS Set (100.60)

K-Number: K241858 · 2024-08-26

Decision Date2024-08-26
Product CodePKL
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

BARS Set (100.60) is a medical device manufactured by Ovesco Endoscopy AG. It received FDA 510(k) clearance on 2024-08-26 under approval number K241858. The device is classified under product code PKL. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BARS Set (100.60)?

BARS Set (100.60) is a medical device that received FDA 510(k) clearance on 2024-08-26. It is manufactured by Ovesco Endoscopy AG. The 510(k) number is K241858.

When was BARS Set (100.60) approved by the FDA?

BARS Set (100.60) received FDA 510(k) clearance on 2024-08-26, under approval number K241858.

What company makes BARS Set (100.60)?

BARS Set (100.60) is manufactured by Ovesco Endoscopy AG.

What is the FDA product code for BARS Set (100.60)?

The FDA product code for BARS Set (100.60) is PKL.

Other Devices by Ovesco Endoscopy AG

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Related Devices (Code: PKL)

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.