510(k) K900645
K900645 is an FDA 510(k) premarket notification submitted by Telectronics Pacing Systems, Inc. for the device "LASERDISH POLYURETHANE VENTRICULAR LEAD W/TRAILING". The FDA issued a decision of Substantially Equivalent on August 8, 1990. The device falls under product code DTB (Permanent Pacemaker Electrode), a Class III device regulated under 21 CFR 870.3680. Telectronics Pacing Systems, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- August 8, 1990
- Date Received
- February 9, 1990
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Permanent Pacemaker Electrode
- Device Class
- Class III
- Regulation Number
- 870.3680
- Review Panel
- CV
- Submission Type