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

ALLIENT SORBENT HEMODIALYSIS SYSTEM, MODEL 1000

K Number: K043574 · Decision Jun 3, 2005
Classifications
1
FEI Numbers
0
Registration Numbers
0
Same Product Code
18
Applicant Total
9
Review Days
158

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Basic Information

Device Name
ALLIENT SORBENT HEMODIALYSIS SYSTEM, MODEL 1000
K Number
K043574
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.5600
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Renal Solutions, Inc.
Date Received
December 27, 2004
Decision Date
June 3, 2005
Product Code
FKT
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
FKT System, Dialysate Delivery, Sorbent Regenerated

Similar 510(k) Clearances

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

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Other Clearances by Renal Solutions, Inc.

K Number Device Name
K123835 2008 HEMODIALYSIS SORBENT SYSTEM
K121497 VENOFER PUMP
K103564 VENOFER PUMP
K093362 2008 HEMODIALYSIS SORBENT SYSTEM
K093964 VENOFER PUMP
K070739 ALLIENT SORBENT HEMODIALYSIS SYSTEM, MODEL# 1500
K060381 ALLIENT SORBET HEMODIALYSIS SYSTEM, MODEL 1100
K031099 SORB+HISORB+CARTRIDGE