DTG · Class I · 21 CFR 870.3690

FDA Product Code DTG: Magnet, Test, Pacemaker

Leading manufacturers include Cyberonics, Inc., Pacesetter Systems and Oscor, Inc..

5
Total
5
Cleared
166d
Avg days
1981
Since

FDA 510(k) Cleared Magnet, Test, Pacemaker Devices (Product Code DTG)

5 devices
1–5 of 5
Cleared Nov 03, 2009
MODEL 220 PATIENT MAGNET
K092364
Cyberonics, Inc.
Cardiovascular · 90d
Cleared Mar 26, 1997
MAGNO ALARM
K960849
Cardiac Assist Devices, Inc.
Cardiovascular · 400d
Cleared Sep 26, 1989
MAESTRO PACEMAKER TEST MAGNET
K895110
Cardiac Control Systems, Inc.
Cardiovascular · 42d
Cleared Mar 12, 1984
IMPLANTABLE ENDOCARDIAL PACING LEADS
K831926
Oscor, Inc.
Cardiovascular · 271d
Cleared Dec 02, 1981
TEST MAGNET
K813153
Pacesetter Systems
Cardiovascular · 26d

About Product Code DTG - Regulatory Context