LIFELINES PHOTIC STIMULATOR— 510(k) K101691
Substantially EquivalentLifelines , Ltd.
FDA 510(k) clearance K101691 for LIFELINES PHOTIC STIMULATOR, Substantially Equivalent on 2010-08-10. Applicant: Lifelines , Ltd..
Clearance details
- Applicant
- Lifelines , Ltd.
- Product code
- Code GWE
- Advisory panel
- Neurology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Crofton, MD, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.