510(k) K872652

UPGRADED AUTO PERITONEAL DIALYSIS CYCLER SYSTEM by Travenol Laboratories, S.A. — Product Code FKX

K872652 is an FDA 510(k) premarket notification submitted by Travenol Laboratories, S.A. for the device "UPGRADED AUTO PERITONEAL DIALYSIS CYCLER SYSTEM". The FDA issued a decision of Substantially Equivalent on September 30, 1987. The device falls under product code FKX (System, Peritoneal, Automatic Delivery), a Class II device regulated under 21 CFR 876.5630. Travenol Laboratories, S.A. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
September 30, 1987
Date Received
July 7, 1987
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

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