RESOLVE UVB PHOTOTHERAPY SYSTEM
FDA 510(k) clearance K072035 · decided 2007-10-16
Clearance details
- K-number
- K072035
- Device name
- RESOLVE UVB PHOTOTHERAPY SYSTEM
- Applicant
- Allux Medical
- Decision
- Substantially Equivalent
- Date received
- 2007-07-25
- Decision date
- 2007-10-16
- Days to decision
- 83 days
- Clearance type
- Traditional
- Product code
- FTC
- Device class
- 2
- Regulation number
- 878.4630
- Medical specialty
- General, Plastic Surgery
- Advisory committee
- General, Plastic Surgery
- Location
- Menlo Park, CA, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.