FDA 510(k)

Ultrasonic Generator

K-Number: K172691 · 2017-10-04

Decision Date2017-10-04

Product CodeLFL

DecisionSubstantially Equivalent

Device Summary

Ultrasonic Generator is a medical device manufactured by Olympus Medical Systems Corp.. It received FDA 510(k) clearance on 2017-10-04 under approval number K172691. The device is classified under product code LFL. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Ultrasonic Generator?

Ultrasonic Generator is a medical device that received FDA 510(k) clearance on 2017-10-04. It is manufactured by Olympus Medical Systems Corp.. The 510(k) number is K172691.

When was Ultrasonic Generator approved by the FDA?

Ultrasonic Generator received FDA 510(k) clearance on 2017-10-04, under approval number K172691.

What company makes Ultrasonic Generator?

Ultrasonic Generator is manufactured by Olympus Medical Systems Corp..

What is the FDA product code for Ultrasonic Generator?

The FDA product code for Ultrasonic Generator is LFL.

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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.