510(k) K884331
K884331 is an FDA 510(k) premarket notification submitted by Medtronic Vascular for the device "MEDTRONIC MODEL 5311B A-V PACING SYSTEM ANALYZER". The FDA issued a decision of Substantially Equivalent on January 10, 1989. The device falls under product code DTC (Analyzer, Pacemaker Generator Function), a Class II device regulated under 21 CFR 870.3630. Medtronic Vascular has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- January 10, 1989
- Date Received
- October 14, 1988
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Analyzer, Pacemaker Generator Function
- Device Class
- Class II
- Regulation Number
- 870.3630
- Review Panel
- CV
- Submission Type