510(k) K790091

AMP AUTOMATIC CYCLER STAND by American Medical Products, Inc. — Product Code KPF

K790091 is an FDA 510(k) premarket notification submitted by American Medical Products, Inc. for the device "AMP AUTOMATIC CYCLER STAND". The FDA issued a decision of Substantially Equivalent on February 16, 1979. The device falls under product code KPF (System, Dialysate Delivery, Semi-Automatic, Peritoneal), a Class II device regulated under 21 CFR 876.5630. American Medical Products, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
February 16, 1979
Date Received
January 16, 1979
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
System, Dialysate Delivery, Semi-Automatic, Peritoneal
Device Class
Class II
Regulation Number
876.5630
Review Panel
GU
Submission Type