Device Classification Name |
Spirometer, Diagnostic
|
510(k) Number |
K873562 |
Device Name |
VITALOGRAPH-ALPHA |
Applicant |
VITALOGRAPH LTD. |
8347 QUIVIRA RD. |
LENEXA,
KS
66215
|
|
Applicant Contact |
LOVINA G FREEMAN |
Correspondent |
VITALOGRAPH LTD. |
8347 QUIVIRA RD. |
LENEXA,
KS
66215
|
|
Correspondent Contact |
LOVINA G FREEMAN |
Regulation Number | 868.1840
|
Classification Product Code |
|
Date Received | 09/02/1987 |
Decision Date | 08/29/1988 |
Decision |
Substantially Equivalent
(SESE) |
Regulation Medical Specialty |
Anesthesiology
|
510k Review Panel |
Anesthesiology
|
Type |
Traditional
|
Reviewed by Third Party |
No
|
Combination Product |
No
|
|
|