IEVA REHABILITATIVE POSITIONAL DEVICE— 510(k) K133990
Substantially EquivalentRemendium Labs, LLC
FDA 510(k) clearance K133990 for IEVA REHABILITATIVE POSITIONAL DEVICE, Substantially Equivalent on 2014-10-09. Applicant: Remendium Labs, LLC.
Clearance details
- Applicant
- Remendium Labs, LLC
- Product code
- Code HIR
- Advisory panel
- Obstetrics/Gynecology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Baton Rouge, LA, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.