Device Classification Name |
automated external defibrillators (non-wearable)
|
510(k) Number |
K932931 |
Device Name |
D1400 DEFIBRILLATOR W/ DEFIBRILLATION ADVISORY OPT |
Applicant |
ZOLL MEDICAL CORP. |
32 SECOND AVE. |
BURLINGTON,
MA
01803
|
|
Applicant Contact |
GARY FREEMAN |
Correspondent |
ZOLL MEDICAL CORP. |
32 SECOND AVE. |
BURLINGTON,
MA
01803
|
|
Correspondent Contact |
GARY FREEMAN |
Regulation Number | 870.5310
|
Classification Product Code |
|
Date Received | 06/16/1993 |
Decision Date | 10/07/1993 |
Decision |
Substantially Equivalent
(SESE) |
Regulation Medical Specialty |
Cardiovascular
|
510k Review Panel |
Cardiovascular
|
Type |
Traditional
|
Reviewed by Third Party |
No
|
Combination Product |
No
|