Device Classification Name |
monitor, breathing frequency
|
510(k) Number |
K981728 |
Device Name |
ALEXANDER MANUFACTURING CO. BATTERY PART NUMBER H134 |
Applicant |
ALEXANDER MFG. CO. |
1511 S GARFIELD PL |
MASON CITY,
IA
50401
|
|
Applicant Contact |
KEN HEIMENDINGER |
Correspondent |
ALEXANDER MFG. CO. |
1511 S GARFIELD PL |
MASON CITY,
IA
50401
|
|
Correspondent Contact |
KEN HEIMENDINGER |
Regulation Number | 868.2375
|
Classification Product Code |
|
Date Received | 05/15/1998 |
Decision Date | 06/26/1998 |
Decision |
SE SUBJECT TO TRACKING REG
(ST) |
Regulation Medical Specialty |
Anesthesiology
|
510k Review Panel |
Anesthesiology
|
Summary |
Summary
|
Type |
Traditional
|
Reviewed by Third Party |
No
|
Combination Product |
No
|
|
|