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

DRAKE WILLOCK REVERSE OSMOSIS WATER TREATMENT SYST

K Number: K894106 · Decision Nov 8, 1989
Classifications
1
FEI Numbers
61
Registration Numbers
61
Same Product Code
116
Applicant Total
11
Review Days
152

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Basic Information

Device Name
DRAKE WILLOCK REVERSE OSMOSIS WATER TREATMENT SYST
K Number
K894106
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.5665
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Applicant
Cd Medical, Inc.
Date Received
June 9, 1989
Decision Date
November 8, 1989
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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K901520 WURTZ CHOLEY CLIP (TM)
K884353 ULTRX(TM) 850 ARTIFICIAL KIDNEY
K880459 480 HIGH-FLOW ULTRAFILTRATION CONTROL DIALYSATE
K873279 8810 PUMP-PUMP SINGLE NEEDLE DEVICE
K864784 SERAFLO(TM) BLOODLINES FOR HEMODIALYSIS
K862304 DRAKE WILLOCK CENTRAL DIALYSATE DELIVERY SYSTEM
K853513 DRAKE WILLOCK 480 UF CONTROL IDALYSATE DELIVERY SY
K844185 MODIFIED C-DAK
Search all 11 clearances from Cd Medical, Inc. →