510(k) K861481

ENDOCARDIAL CARBON-TIP LEAD by Pacesetter Systems — Product Code DTB

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