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FDA 510(k)

Centurion™ Vision System (Active Sentry™) (8065753057)

K-Number: K233902 · 2024-01-10

Decision Date2024-01-10
Product CodeHQC
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

Centurion™ Vision System (Active Sentry™) (8065753057) is a medical device manufactured by Alcon Laboratories, Inc.. It received FDA 510(k) clearance on 2024-01-10 under approval number K233902. The device is classified under product code HQC. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Centurion™ Vision System (Active Sentry™) (8065753057)?

Centurion™ Vision System (Active Sentry™) (8065753057) is a medical device that received FDA 510(k) clearance on 2024-01-10. It is manufactured by Alcon Laboratories, Inc.. The 510(k) number is K233902.

When was Centurion™ Vision System (Active Sentry™) (8065753057) approved by the FDA?

Centurion™ Vision System (Active Sentry™) (8065753057) received FDA 510(k) clearance on 2024-01-10, under approval number K233902.

What company makes Centurion™ Vision System (Active Sentry™) (8065753057)?

Centurion™ Vision System (Active Sentry™) (8065753057) is manufactured by Alcon Laboratories, Inc..

What is the FDA product code for Centurion™ Vision System (Active Sentry™) (8065753057)?

The FDA product code for Centurion™ Vision System (Active Sentry™) (8065753057) is HQC.

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Official Source

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