FDA 510(k)

Sonic Window

K-Number: K161342 · 2016-06-15

Decision Date2016-06-15

Product CodeIYO

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

Sonic Window is a medical device manufactured by Analogic Corporation. It received FDA 510(k) clearance on 2016-06-15 under approval number K161342. The device is classified under product code IYO. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Sonic Window?

Sonic Window is a medical device that received FDA 510(k) clearance on 2016-06-15. It is manufactured by Analogic Corporation. The 510(k) number is K161342.

When was Sonic Window approved by the FDA?

Sonic Window received FDA 510(k) clearance on 2016-06-15, under approval number K161342.

What company makes Sonic Window?

Sonic Window is manufactured by Analogic Corporation.

What is the FDA product code for Sonic Window?

The FDA product code for Sonic Window is IYO.

Other Devices by Analogic Corporation

K182147CTXX85 K172058CT6485, CT12885 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.