510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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DTGClass I

Magnet, Test, Pacemaker

21 CFR 870.3690 / Cardiovascular
FDA source (opens on fda.gov)

DTG is the FDA product code for Magnet, Test, Pacemaker, a class I device type, regulated under 21 CFR 870.3690. As of , FDA records hold 5 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
DTG
Device name
Magnet, Test, Pacemaker
Regulation
21 CFR 870.3690
Device class
Class I
Review panel
Cardiovascular
Submission type
510(k) exempt
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
5
Ingested recalls
0

Clearances, product code DTG

By decision year
5 clearances under product code DTG with a decision year between 1981 and 2009, 1981 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code DTG by decision year
YearClearances
19811
19841
19891
19971
20091

Applicants with the most clearances

Product code DTG
Applicants holding the most 510(k) clearances under product code DTG
ApplicantClearances
Cardiac Assist Devices, Inc.1
Cardiac Control Systems, Inc.1
LivaNova USA, Inc.1
Oscor Inc.1
Pacesetter Systems1

Companies listing this code with FDA

Companies whose registered establishments list this code