PREMIER III PHASED ARRAY CTL SPINE COIL— 510(k) K030042
Substantially EquivalentUsa Instruments, Inc.
FDA 510(k) clearance K030042 for PREMIER III PHASED ARRAY CTL SPINE COIL, Substantially Equivalent on 2003-02-24. Applicant: Usa Instruments, Inc..
Clearance details
- Applicant
- Usa Instruments, Inc.
- Product code
- Code MOS
- Advisory panel
- Radiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Aurora, OH, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.