Capillus 112, Capillus 244— 510(k) K192012
Substantially EquivalentCapillus
FDA 510(k) clearance K192012 for Capillus 112, Capillus 244, Substantially Equivalent on 2019-09-12. Applicant: Capillus. Device class: 2.
Clearance details
- Applicant
- Capillus
- 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
- Special
- Location
- Miami, FL, US
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Data sourced from openFDA. This site is unofficial and independent of the FDA.