Device
Atlas
510(k)
Recalls
Companies
Specialties
Home
›
Companies
›
Sulzer Oscor, Inc.
Sulzer Oscor, Inc.
Medical device manufacturer in Palm Harbor, FL.
2
510(k) clearances
0
PMA approvals
0
recalls
Device types
DTE Pulse-Generator, Pacemaker, External
1
DTB Permanent Pacemaker Electrode
1
510(k) clearances
510(k)
Device
Decision
K990142
HT, Model HT PB
DTB · Traditional
07/30/1999
ST
K970497
Pace 101H
DTE · Traditional
06/04/1997
SE