Device Classification Name |
Vaporizer, Anesthesia, Non-Heated
|
510(k) Number |
K953748 |
Device Name |
TECHNOFIL |
Applicant |
TECHNIMECA MEDIC, INC. |
2300 COHEN |
ST. LAURENT, QUEBEC,
CA
H4R 2N8
|
|
Applicant Contact |
JACQUES ROBERGE |
Correspondent |
TECHNIMECA MEDIC, INC. |
2300 COHEN |
ST. LAURENT, QUEBEC,
CA
H4R 2N8
|
|
Correspondent Contact |
JACQUES ROBERGE |
Regulation Number | 868.5880
|
Classification Product Code |
|
Date Received | 08/11/1995 |
Decision Date | 01/25/1996 |
Decision |
Substantially Equivalent
(SESE) |
Regulation Medical Specialty |
Anesthesiology
|
510k Review Panel |
Anesthesiology
|
Type |
Traditional
|
Reviewed by Third Party |
No
|
Combination Product |
No
|
|
|