510(k) K944966
K944966 is an FDA 510(k) premarket notification submitted by Medtronic Blood Systems, Inc. for the device "UNIPOLAR ATRIAL TEMPORARY PACING LEAD,MODEL 6492". The FDA issued a decision of Substantially Equivalent on July 14, 1995. The device falls under product code LDF (Electrode, Pacemaker, Temporary), a Class II device regulated under 21 CFR 870.3680. Medtronic Blood Systems, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- July 14, 1995
- Date Received
- October 11, 1994
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Electrode, Pacemaker, Temporary
- Device Class
- Class II
- Regulation Number
- 870.3680
- Review Panel
- CV
- Submission Type