510(k) Premarket Notification Database
Device Classification Name |
system, dialysate delivery, central multiple patient
|
510(k) Number | K840814 |
Device Name | HOSPAL MODEL H1210 |
Applicant |
|
Contact | |
Regulation Number | 876.5820 |
Classification Product Code |
|
Date Received | 02/17/1984 |
Decision Date | 04/02/1984 |
Decision |
substantially equivalent (SE) |
Classification Advisory Committee |
Gastroenterology/Urology
|
Review Advisory Committee |
Gastroenterology/Urology
|
Statement/Summary/Purged Status |
Purged, no summary or statement
|
Type |
Traditional
|
Reviewed by Third Party |
No
|
Expedited Review |
|
|
|