510(k) K942440

AFP CARDIAC PACING SYSTEM MODEL 283 by Siemens-Pacesetter, Inc. — Product Code DTB

K942440 is an FDA 510(k) premarket notification submitted by Siemens-Pacesetter, Inc. for the device "AFP CARDIAC PACING SYSTEM MODEL 283". The FDA issued a decision of ST on August 8, 1994. The device falls under product code DTB (Permanent Pacemaker Electrode), a Class III device regulated under 21 CFR 870.3680. Siemens-Pacesetter, Inc. has at least 6 other 510(k) clearances on record.

Clearance Details

Decision
ST ()
Decision Date
August 8, 1994
Date Received
May 20, 1994
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