Clearance Summary
SONICATOR PLUS 930, MODEL ME 930 received FDA 510(k) clearance under submission number K013192, sponsored by Mettler Electronics Corp.. The device was reviewed via the Abbreviated premarket notification pathway and assigned to the Physical Medicine review panel. The statutory decision date of record is 2001-10-17.
- Submission: K013192
- Applicant / Sponsor: Mettler Electronics Corp.
- Clearance pathway: Abbreviated
- Review panel: Physical Medicine
- Device class: Class II
- Regulation citation: 21 CFR 890.5300
- Decision date: 2001-10-17
Classification & Regulation
This clearance is catalogued under FDA product code IMI and 21 CFR 890.5300, within the Physical Medicine review panel as a Class II device.