510(k) K780368
K780368 is an FDA 510(k) premarket notification submitted by Medtronic Vascular for the device "MODUMED MUGX". The FDA issued a decision of Substantially Equivalent on March 14, 1978. The device falls under product code JWM (System, Tomographic, Nuclear), a Class II device regulated under 21 CFR 892.1310. Medtronic Vascular has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- March 14, 1978
- Date Received
- March 7, 1978
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- System, Tomographic, Nuclear
- Device Class
- Class II
- Regulation Number
- 892.1310
- Review Panel
- RA
- Submission Type