MISONIX INC. SONATHERM 600 ULTRASONIC LESION GENERATING SYSTEM
FDA 510(k) clearance K042096 · decided 2006-01-26
Clearance details
- K-number
- K042096
- Device name
- MISONIX INC. SONATHERM 600 ULTRASONIC LESION GENERATING SYSTEM
- Applicant
- Misonix, Inc.
- Decision
- Substantially Equivalent
- Date received
- 2004-08-04
- Decision date
- 2006-01-26
- Days to decision
- 540 days
- Clearance type
- Traditional
- Product code
- NTB
- Device class
- 2
- Regulation number
- 878.4400
- Medical specialty
- General, Plastic Surgery
- Advisory committee
- General, Plastic Surgery
- Location
- Farmingdale, NY, US
- Third-party review
- No
- Expedited review
- No
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Similar devices under this product code
Devices cleared under the same product code - the starting set for predicate research.
| Record | Firm | Date |
|---|---|---|
| TheraVision Ultrasound Ablation System and ACOUSTx Applicators (K150019) | Acoustic Medsystems, Inc. | 2016-01-13 |
| SONATHERM 600I ULTRASONIC LESION GENERATING SYSTEM (K070779) | Misonix, Inc. | 2008-07-09 |
| ULTRAZONIX SPINE MINIMAL-INVASIVE DISC SYSTEM (K060346) | Ultrazonix Dnt AB | 2006-12-22 |
| ULTRACINCH ABLATION DEVICE, ULTRACINCH ACCESSORY PACK, MODELS UC-8, UC-9, UC-10, UC-11, UC-12, UC-13, UC-14, UC-ACC-1 (K040641) | Epicor Medical, Inc. | 2004-05-05 |
| EPICOR MEDICAL ABLATION SYSTEM (K022894) | Epicor Medical, Inc. | 2004-02-26 |
Recalls involving this device
No recalls on record reference this clearance.