FDA 510(k) FDA class 2 Unknown 🇺🇸 United States

CD HOME DIALYSERVICE HEMODIALYSIS TRAY

K Number: K925654 · Decision Mar 30, 1994
Classifications
1
FEI Numbers
49
Registration Numbers
49
Same Product Code
181
Applicant Total
11
Review Days
506

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Basic Information

Device Name
CD HOME DIALYSERVICE HEMODIALYSIS TRAY
K Number
K925654
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.5820
Medical Specialty
Gastroenterology, Urology
Decision
Unknown
Statement or Summary
Summary
Applicant
Cd Medical, Inc.
Date Received
November 9, 1992
Decision Date
March 30, 1994
Product Code
KOC
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
KOC Accessories, Blood Circuit, Hemodialysis

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Other Clearances by Cd Medical, Inc.

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K894106 DRAKE WILLOCK REVERSE OSMOSIS WATER TREATMENT SYST
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. →