510(k) K000345
K000345 is an FDA 510(k) premarket notification submitted by Medical Advances, Inc. for the device "MULTI PURPOSE FLEX ARRAY COIL : MODEL 235 SERIES". The FDA issued a decision of Substantially Equivalent on Apr 11, 2000. The device falls under product code MOS (Coil, Magnetic Resonance, Specialty), a Class II device regulated under 21 CFR 892.1000. Medical Advances, Inc. has 56 other 510(k) clearances on record.
Clearance details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Apr 11, 2000
- Date Received
- Feb 3, 2000
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device classification
- Device Name
- Coil, Magnetic Resonance, Specialty
- Device Class
- Class II
- Regulation Number
- 892.1000
- Review Panel
- RA
- Submission Type
- 510(k)