MISONIX INC. SONATHERM 600 ULTRASONIC LESION GENERATING SYSTEM— 510(k) K042096
Substantially EquivalentMisonix, Inc.
FDA 510(k) clearance K042096 for MISONIX INC. SONATHERM 600 ULTRASONIC LESION GENERATING SYSTEM, Substantially Equivalent on 2006-01-26. Applicant: Misonix, Inc.. Device class: 2.
Clearance details
- Applicant
- Misonix, Inc.
- Product code
- Code NTB
- Device class
- Class 2
- Regulation
- 21 CFR 878.4400
- Advisory panel
- General, Plastic Surgery
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Farmingdale, NY, US
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