3.0T Air MP M, 3.0T Air MP L— 510(k) K182504
Substantially EquivalentGe Healthcare Coils (Usa Instruments, Inc.)
FDA 510(k) clearance K182504 for 3.0T Air MP M, 3.0T Air MP L, Substantially Equivalent on 2018-10-12. Applicant: Ge Healthcare Coils (Usa Instruments, Inc.). Device class: 2.
Clearance details
- Applicant
- Ge Healthcare Coils (Usa Instruments, Inc.)
- Product code
- Code MOS
- Device class
- Class 2
- Regulation
- 21 CFR 892.1000
- Advisory panel
- Radiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Aurora, OH, US
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More clearances from Ge Healthcare Coils (Usa Instruments, Inc.)
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