Nutra Light Advanced
FDA 510(k) clearance K150370 · decided 2015-07-22
Clearance details
- K-number
- K150370
- Device name
- Nutra Light Advanced
- Applicant
- Nutra Luxe MD, LLC
- Decision
- Substantially Equivalent
- Date received
- 2015-02-13
- Decision date
- 2015-07-22
- Days to decision
- 159 days
- Clearance type
- Traditional
- Product code
- OLP
- Device class
- 2
- Regulation number
- 878.4810
- Medical specialty
- General, Plastic Surgery
- Advisory committee
- General, Plastic Surgery
- Location
- Fort Myers, FL, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.