Ultrasonic Generator
K-Number: K172691 · 2017-10-04
Device Summary
Frequently Asked Questions
What is the Ultrasonic Generator?
Ultrasonic Generator is a medical device that received FDA 510(k) clearance on 2017-10-04. The listed applicant is Olympus Medical Systems Corp.. The 510(k) number is K172691.
When did Ultrasonic Generator receive FDA 510(k) clearance?
Ultrasonic Generator received FDA 510(k) clearance on 2017-10-04, under 510(k) number K172691.
Who is the listed applicant for Ultrasonic Generator?
The FDA 510(k) record lists Olympus Medical Systems Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Ultrasonic Generator?
The FDA product code for Ultrasonic Generator is LFL.
Other records listing Olympus Medical Systems Corp. as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: LFL)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
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.