510(k) K861481
K861481 is an FDA 510(k) premarket notification submitted by Pacesetter Systems for the device "ENDOCARDIAL CARBON-TIP LEAD". The FDA issued a decision of Substantially Equivalent on June 6, 1986. The device falls under product code DTB (Permanent Pacemaker Electrode), a Class III device regulated under 21 CFR 870.3680. Pacesetter Systems has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- June 6, 1986
- Date Received
- April 22, 1986
- 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