FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

CARDIOFLOW 100 HEMOCONCENTRATOR/PREPARATION KIT

K Number: K883307 · Decision Oct 12, 1988
Classifications
1
FEI Numbers
89
Registration Numbers
89
Same Product Code
343
Applicant Total
55
Review Days
69

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Basic Information

Device Name
CARDIOFLOW 100 HEMOCONCENTRATOR/PREPARATION KIT
K Number
K883307
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.5860
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Applicant
Hospal Medical Corp.
Date Received
August 4, 1988
Decision Date
October 12, 1988
Product Code
KDI
Advisory Committee
Gastroenterology, Urology
Review Advisory Committee
GU
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
KDI Dialyzer, High Permeability With Or Without Sealed Dialysate System

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (KDI), ordered by most recent decision date.

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Other Clearances by Hospal Medical Corp.

K Number Device Name
K893742 FILTRAL TM 20 HEMODIALYZER/FILTER
K884365 MULTIFLOW(TM) 60 KIT
K884326 FILTRAL TM 8 HEMODIALYZER
K872767 FILTRAL 10, FILTRAL 12, FILTRAL 16 HEMODIALYZER
K871218 MONITRAL S GS HEMODIALYSIS SINGLE PATIENT UNIT
K863961 HOSPAL BIOSPAL 1800S
K863592 DISSCAP 80E, 110E, 140E, 160E
K861156 HOSPAL DIALYSATE FOR CAVHD
K861230 MONITRAL S
K854951 PLUME Y SET
Search all 55 clearances from Hospal Medical Corp. →