Device Classification Name |
transmitters and receivers, physiological signal, radiofrequency
|
510(k) Number |
K061606 |
Device Name |
DEFIBRILLATOR CABLE TESTER, MODEL DT2200 |
Applicant |
MEDICAL DEVICES/PADPRO, INC. |
PO BOX 7007 |
DEERFIELD,
IL
60015
|
|
Applicant Contact |
DANIEL KAMM |
Correspondent |
REGULATORY TECHNOLOGY SERVICES, LLC |
1000 Westgate Drive, |
Suite 510k |
Saint Paul,
MN
55114
|
|
Correspondent Contact |
MARK JOB |
Regulation Number | 870.2910
|
Classification Product Code |
|
Date Received | 06/09/2006 |
Decision Date | 06/21/2006 |
Decision |
Substantially Equivalent
(SESE) |
Regulation Medical Specialty |
Cardiovascular
|
510k Review Panel |
Cardiovascular
|
Summary |
Summary
|
Type |
Traditional
|
Reviewed by Third Party |
Yes
|
Combination Product |
No
|
|
|