FLEX ARM RETRACTOR SYSTEM— 510(k) K071338
Substantially EquivalentKoros USA, Inc.
FDA 510(k) clearance K071338 for FLEX ARM RETRACTOR SYSTEM, Substantially Equivalent on 2007-05-29. Applicant: Koros USA, Inc..
Clearance details
- Applicant
- Koros USA, Inc.
- Product code
- Code GZT
- Advisory panel
- Neurology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Moorepark, CA, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.