OPART, MODEL MRT-600— 510(k) K002522
Substantially EquivalentToshiba America Mri, Inc.
FDA 510(k) clearance K002522 for OPART, MODEL MRT-600, Substantially Equivalent on 2000-10-25. 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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