FLEXART QD HEAD/NECK COIL— 510(k) K961391
Substantially EquivalentToshiba America Mri, Inc.
FDA 510(k) clearance K961391 for FLEXART QD HEAD/NECK COIL, Substantially Equivalent on 1996-07-09. Applicant: Toshiba America Mri, Inc.. Device class: 2.
Clearance details
- Applicant
- Toshiba America Mri, 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
- S. San Francisco, CA, US
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More clearances from Toshiba America Mri, Inc.
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