LaserCap LC Pro and LC Elite— 510(k) K150613
Substantially EquivalentTransdermal Cap, Inc.
FDA 510(k) clearance K150613 for LaserCap LC Pro and LC Elite, Substantially Equivalent on 2015-07-22. Applicant: Transdermal Cap, Inc.. Device class: 2.
Clearance details
- Applicant
- Transdermal Cap, Inc.
- Product code
- Code OAP
- Device class
- Class 2
- Regulation
- 21 CFR 890.5500
- Advisory panel
- Physical Medicine
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Cleveland, OH, US
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More clearances from Transdermal Cap, Inc.
view allData sourced from openFDA. This site is unofficial and independent of the FDA.