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FDA 510(k)

Katalyst Cyclophotocoagulation Probe

K-Number: K163632 · 2017-06-15

ApplicantKatalyst Surgical, LLC
Decision Date2017-06-15
Product CodeLQJ
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

Katalyst Cyclophotocoagulation Probe is a medical device manufactured by Katalyst Surgical, LLC. It received FDA 510(k) clearance on 2017-06-15 under approval number K163632. The device is classified under product code LQJ. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Katalyst Cyclophotocoagulation Probe?

Katalyst Cyclophotocoagulation Probe is a medical device that received FDA 510(k) clearance on 2017-06-15. It is manufactured by Katalyst Surgical, LLC. The 510(k) number is K163632.

When was Katalyst Cyclophotocoagulation Probe approved by the FDA?

Katalyst Cyclophotocoagulation Probe received FDA 510(k) clearance on 2017-06-15, under approval number K163632.

What company makes Katalyst Cyclophotocoagulation Probe?

Katalyst Cyclophotocoagulation Probe is manufactured by Katalyst Surgical, LLC.

What is the FDA product code for Katalyst Cyclophotocoagulation Probe?

The FDA product code for Katalyst Cyclophotocoagulation Probe is LQJ.

Other Devices by Katalyst Surgical, LLC

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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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