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FDA 510(k)

CENTURION Vision System (Active SentryTM)

K-Number: K161794 · 2017-04-14

ApplicantAlcon Research, Ltd.
Decision Date2017-04-14
Product CodeHQC
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

CENTURION Vision System (Active SentryTM) is a medical device manufactured by Alcon Research, Ltd.. It received FDA 510(k) clearance on 2017-04-14 under approval number K161794. 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 SentryTM)?

CENTURION Vision System (Active SentryTM) is a medical device that received FDA 510(k) clearance on 2017-04-14. It is manufactured by Alcon Research, Ltd.. The 510(k) number is K161794.

When was CENTURION Vision System (Active SentryTM) approved by the FDA?

CENTURION Vision System (Active SentryTM) received FDA 510(k) clearance on 2017-04-14, under approval number K161794.

What company makes CENTURION Vision System (Active SentryTM)?

CENTURION Vision System (Active SentryTM) is manufactured by Alcon Research, Ltd..

What is the FDA product code for CENTURION Vision System (Active SentryTM)?

The FDA product code for CENTURION Vision System (Active SentryTM) is HQC.

Related Clinical Trials

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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.

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