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FDA 510(k)

CS 9600

K-Number: K200183 · 2020-03-13

ApplicantTrophy
Decision Date2020-03-13
Product CodeOAS
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

CS 9600 is a medical device manufactured by Trophy. It received FDA 510(k) clearance on 2020-03-13 under approval number K200183. The device is classified under product code OAS. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CS 9600?

CS 9600 is a medical device that received FDA 510(k) clearance on 2020-03-13. It is manufactured by Trophy. The 510(k) number is K200183.

When was CS 9600 approved by the FDA?

CS 9600 received FDA 510(k) clearance on 2020-03-13, under approval number K200183.

What company makes CS 9600?

CS 9600 is manufactured by Trophy.

What is the FDA product code for CS 9600?

The FDA product code for CS 9600 is OAS.

Related Clinical Trials

Other Devices by Trophy

Related Devices (Code: OAS)

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.