Device Classification Name |
airway, esophageal (obturator)
|
510(k) Number |
K864200 |
Device Name |
VETA/VENTED ESOPHAGEAL TUBE AIRWAY |
Applicant |
CRANCO CO. |
120 OAKWOOD PLAZA |
5320 SOUTH 900 EAST |
SALT LAKE CITY,
UT
84117
|
|
Applicant Contact |
RICHARD CRANGLE |
Correspondent |
CRANCO CO. |
120 OAKWOOD PLAZA |
5320 SOUTH 900 EAST |
SALT LAKE CITY,
UT
84117
|
|
Correspondent Contact |
RICHARD CRANGLE |
Regulation Number | 868.5650
|
Classification Product Code |
|
Date Received | 10/27/1986 |
Decision Date | 03/17/1987 |
Decision |
Substantially Equivalent
(SESE) |
Regulation Medical Specialty |
Anesthesiology
|
510k Review Panel |
Anesthesiology
|
Type |
Traditional
|
Reviewed by Third Party |
No
|
Combination Product |
No
|
|
|