FDA 510(k)

CT6485, CT12885

K-Number: K172058 · 2018-02-13

Decision Date2018-02-13

Product CodeJAK

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

CT6485, CT12885 is a medical device manufactured by Analogic Corporation. It received FDA 510(k) clearance on 2018-02-13 under approval number K172058. The device is classified under product code JAK. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CT6485, CT12885?

CT6485, CT12885 is a medical device that received FDA 510(k) clearance on 2018-02-13. It is manufactured by Analogic Corporation. The 510(k) number is K172058.

When was CT6485, CT12885 approved by the FDA?

CT6485, CT12885 received FDA 510(k) clearance on 2018-02-13, under approval number K172058.

What company makes CT6485, CT12885?

CT6485, CT12885 is manufactured by Analogic Corporation.

What is the FDA product code for CT6485, CT12885?

The FDA product code for CT6485, CT12885 is JAK.

Other Devices by Analogic Corporation

K161342Sonic Window K182147CTXX85 K201231CTxx85 CT Scanner

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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.