Device Classification Name |
connector, airway (extension)
|
510(k) Number |
K931216 |
Device Name |
CONNECTORS AND AIRWAY EXTENSIONS |
Applicant |
TEKNOR MEDICAL PRODUCTS, INC. |
P.O. BOX 22017 |
TRENTON, ONTARIO,
CA
K8V 6S3
|
|
Applicant Contact |
PETER F HUFF |
Correspondent |
TEKNOR MEDICAL PRODUCTS, INC. |
P.O. BOX 22017 |
TRENTON, ONTARIO,
CA
K8V 6S3
|
|
Correspondent Contact |
PETER F HUFF |
Regulation Number | 868.5810
|
Classification Product Code |
|
Date Received | 03/10/1993 |
Decision Date | 04/23/1993 |
Decision |
Substantially Equivalent
(SESE) |
Regulation Medical Specialty |
Anesthesiology
|
510k Review Panel |
Anesthesiology
|
Type |
Traditional
|
Reviewed by Third Party |
No
|
Combination Product |
No
|
|
|