ACLEARA, THERACLEAR— 510(k) K123889
Substantially EquivalentTheravant Corporation
FDA 510(k) clearance K123889 for ACLEARA, THERACLEAR, Substantially Equivalent on 2013-03-04. Applicant: Theravant Corporation. Device class: 2.
Clearance details
- Applicant
- Theravant Corporation
- Product code
- Code ONF
- Device class
- Class 2
- Regulation
- 21 CFR 878.4810
- Advisory panel
- General, Plastic Surgery
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Cary, NC, US
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