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

WATER PURIFICATION SYSTEM FOR HEMODIALYSIS

K Number: K920186 · Decision Jun 13, 1995
Classifications
1
FEI Numbers
61
Registration Numbers
61
Same Product Code
116
Applicant Total
4
Review Days
1246

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Basic Information

Device Name
WATER PURIFICATION SYSTEM FOR HEMODIALYSIS
K Number
K920186
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.5665
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Better Water, Inc.
Date Received
January 14, 1992
Decision Date
June 13, 1995
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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Other Clearances by Better Water, Inc.

K Number Device Name
K051620 MATRIX DIGITAL REVERSE OSMOSIS WATER TREATMENT SYSTEM, MODEL EQRMD SERIES
K992793 SODIUM BICARBONATE MIXING/DELIVERY SYSTEM, AND THE CONCENTRATE DELIVERY SYSTEM
K954928 PORTABLE REVERSE OSMOSIS MACHINE