Device Classification Name |
tube, double lumen for intestinal decompression and/or intubation
|
510(k) Number |
K880850 |
Device Name |
KEITH NASOGASTRIC SUMP TUBE W/ANTI-REFLUX VALVE |
Applicant |
KMB MEDICAL PRODUCTS CO. |
320 BROOKES DRIVE, STE. 110 |
HAZELWOOD,
MO
63042
|
|
Applicant Contact |
C. W KEITH |
Correspondent |
KMB MEDICAL PRODUCTS CO. |
320 BROOKES DRIVE, STE. 110 |
HAZELWOOD,
MO
63042
|
|
Correspondent Contact |
C. W KEITH |
Regulation Number | 876.5980
|
Classification Product Code |
|
Date Received | 03/01/1988 |
Decision Date | 05/26/1988 |
Decision |
Substantially Equivalent
(SESE) |
Regulation Medical Specialty |
Gastroenterology/Urology
|
510k Review Panel |
Gastroenterology/Urology
|
Type |
Traditional
|
Reviewed by Third Party |
No
|
Combination Product |
No
|
|
|