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

FRESENIUS HEMOFLOW F50 & F70

K Number: K864169 · Decision Nov 6, 1986
Classifications
1
FEI Numbers
89
Registration Numbers
89
Same Product Code
343
Applicant Total
21
Review Days
13

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Basic Information

Device Name
FRESENIUS HEMOFLOW F50 & F70
K Number
K864169
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.5860
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Applicant
Seratronics, Inc.
Date Received
October 24, 1986
Decision Date
November 6, 1986
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 Seratronics, Inc.

K Number Device Name
K955299 DPS 4 DIALYZER PREPARATION SYSTEM
K931336 DRS 4 DIALYZER REPROCESSING SYSTEM
K944539 DRS 4 ND DIALYZER REPROCESSING SYSTEM
K923529 DMS DATA MANAGEMENT SYSTEM/DRS-4 DIALYZER REPROCES
K914580 DRS-4 DIALYZER REPROCESSING SYSTEM
K874573 FRESENIUS PURISTERIL 340 (TM)
K874872 FRESENIUS HEMOFLOW F3, F4, F5, F7
K870725 FRESENIUS HEMOFLOW F6 AND F8
K870724 FRESENIUS HEMOFLOW F60 AND F80
K864587 FRESENIUS ULTRAFLUX AV400, AV600
Search all 21 clearances from Seratronics, Inc. →