MODELS 4100 AND 4300 MULTITHERAPY— 510(k) K945954
Substantially EquivalentSpinalight, Inc.
FDA 510(k) clearance K945954 for MODELS 4100 AND 4300 MULTITHERAPY, Substantially Equivalent on 1995-01-19. Applicant: Spinalight, Inc..
Clearance details
- Applicant
- Spinalight, Inc.
- Product code
- Code JFB
- Advisory panel
- Physical Medicine
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Woodstock, GA, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.