Device Classification Name |
automated external defibrillators (non-wearable)
|
510(k) Number |
K072596 |
Device Name |
LIFE+CEL OR LIFECEL BATTERY PACK, MODEL 5L500 |
Applicant |
AMCO INTERNATIONAL MANUFACTURING & DESIGN, INC. |
377 ZANE CT. |
ELIZABETH,
CO
80107
|
|
Applicant Contact |
ALEXANDER B HENDERSON |
Correspondent |
AMCO INTERNATIONAL MANUFACTURING & DESIGN, INC. |
377 ZANE CT. |
ELIZABETH,
CO
80107
|
|
Correspondent Contact |
ALEXANDER B HENDERSON |
Regulation Number | 870.5310
|
Classification Product Code |
|
Date Received | 09/14/2007 |
Decision Date | 01/24/2008 |
Decision |
Substantially Equivalent
(SESE) |
Regulation Medical Specialty |
Cardiovascular
|
510k Review Panel |
Cardiovascular
|
Summary |
Summary
|
Type |
Traditional
|
Reviewed by Third Party |
No
|
Combination Product |
No
|
|
|