510(k) K082373
K082373 is an FDA 510(k) premarket notification submitted by Noras Mri Products GmbH for the device "NORAS MR-BI320-PA 3T". The FDA issued a decision of Substantially Equivalent on August 29, 2008. The device falls under product code MOS (Coil, Magnetic Resonance, Specialty), a Class II device regulated under 21 CFR 892.1000. Noras Mri Products GmbH has at least 9 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- August 29, 2008
- Date Received
- August 18, 2008
- Clearance Type
- Abbreviated
- Expedited Review
- No
- Third Party Review
- Yes
Device Classification
- Device Name
- Coil, Magnetic Resonance, Specialty
- Device Class
- Class II
- Regulation Number
- 892.1000
- Review Panel
- RA
- Submission Type