Device Classification Name |
Spirometer, Diagnostic
|
510(k) Number |
K822861 |
Device Name |
LIFELINE 4800-C DIGITAL SPIROMETER |
Applicant |
LIFELINE CONTROLS |
4221 Richmond Rd., N.W. |
Walker,
MI
49534
|
|
Correspondent |
LIFELINE CONTROLS |
4221 Richmond Rd., N.W. |
Walker,
MI
49534
|
|
Regulation Number | 868.1840
|
Classification Product Code |
|
Date Received | 09/27/1982 |
Decision Date | 11/03/1982 |
Decision |
Substantially Equivalent
(SESE) |
Regulation Medical Specialty |
Anesthesiology
|
510k Review Panel |
Anesthesiology
|
Type |
Traditional
|
Reviewed by Third Party |
No
|
Combination Product |
No
|
|
|