ULTRASONIC SURGERY— 510(k) K121620

Substantially Equivalent

Dmetec.Co., Ltd.

FDA 510(k) clearance K121620 for ULTRASONIC SURGERY, Substantially Equivalent on 2012-12-11. Applicant: Dmetec.Co., Ltd.. Device class: 2.

Clearance details

Applicant: Dmetec.Co., Ltd.
Product code: Code DZI
Device class: Class 2
Regulation: 21 CFR 872.4120
Advisory panel: Dental
Date received: 2012-06-01
Decision date: 2012-12-11
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Los Angeles, CA, US

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.