Device Classification Name |
Percussor, Powered-Electric
|
510(k) Number |
K931988 |
Device Name |
3P (PULMONARY PERCUSSIVE PACK) |
Applicant |
DELTA MEDICAL MANUF, INC. |
P.O. BOX 52038 |
RALEIGH,
NC
27612
|
|
Applicant Contact |
DEN RAVELY |
Correspondent |
DELTA MEDICAL MANUF, INC. |
P.O. BOX 52038 |
RALEIGH,
NC
27612
|
|
Correspondent Contact |
DEN RAVELY |
Regulation Number | 868.5665
|
Classification Product Code |
|
Date Received | 04/22/1993 |
Decision Date | 10/28/1994 |
Decision |
Substantially Equivalent
(SESE) |
Regulation Medical Specialty |
Anesthesiology
|
510k Review Panel |
Anesthesiology
|
Type |
Traditional
|
Reviewed by Third Party |
No
|
Combination Product |
No
|
|
|