LINEAR LIFT DEVICE— 510(k) K881676
Substantially EquivalentCybex
FDA 510(k) clearance K881676 for LINEAR LIFT DEVICE, Substantially Equivalent on 1990-04-25. Applicant: Cybex.
Clearance details
- Applicant
- Cybex
- Product code
- Code IKK
- Advisory panel
- Physical Medicine
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Ronkonkoma, NY, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.