Device Classification Name |
Vaporizer, Anesthesia, Non-Heated
|
510(k) Number |
K884090 |
Device Name |
LUNDY VAPORIZER SYSTEM |
Applicant |
VAPORFLOW TECHNOLOGY, INC. |
1731 SAYBROOK LN. |
TUSTIN,
CA
92680
|
|
Applicant Contact |
JOHN C LUNDY |
Correspondent |
VAPORFLOW TECHNOLOGY, INC. |
1731 SAYBROOK LN. |
TUSTIN,
CA
92680
|
|
Correspondent Contact |
JOHN C LUNDY |
Regulation Number | 868.5880 |
Classification Product Code |
|
Date Received | 09/28/1988 |
Decision Date | 01/24/1989 |
Decision |
Substantially Equivalent
(SESE) |
Regulation Medical Specialty |
Anesthesiology
|
510k Review Panel |
Anesthesiology
|
Type |
Traditional
|
Reviewed by Third Party |
No
|
Combination Product |
No
|
Predetermined Change Control Plan Authorized |
No
|
|
|