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

NEPHROS DSU FILTER, NEPHROS MSU FILTER, NEPHROS SSU FILTER

K Number: K110285 · Decision Jul 14, 2011
Classifications
1
FEI Numbers
61
Registration Numbers
61
Same Product Code
116
Applicant Total
8
Review Days
164

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Basic Information

Device Name
NEPHROS DSU FILTER, NEPHROS MSU FILTER, NEPHROS SSU FILTER
K Number
K110285
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
876.5665
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Nephros, Inc.
Date Received
January 31, 2011
Decision Date
July 14, 2011
Product Code
FIP
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
FIP Subsystem, Water Purification

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K Number Device Name
K161304 EndoPur Filter
K161467 HydraGuard 10 UltraFilter
K153084 Nephros S100
K141731 NEPHROS DSU-H, NEPHROS SSU-H
K112314 NEPHROS OLPUR H2H HEMODIAFILTRATION (HDF) MODULE AND OLPUR MD 220 HEMODIAFILTER
K090885 NEPHROS, INC., DSU DUAL STAGE ULTRAFILTER
K050603 OLPUR DIALYZER, MODEL HD 190