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

AUTOMATIC PERITONEAL DIALYSIS CYCLER SET (5C4437)

K Number: K873984 · Decision Oct 20, 1987
Classifications
1
FEI Numbers
24
Registration Numbers
24
Same Product Code
112
Applicant Total
206
Review Days
20

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Basic Information

Device Name
AUTOMATIC PERITONEAL DIALYSIS CYCLER SET (5C4437)
K Number
K873984
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.5630
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Applicant
Travenol Laboratories, S.A.
Date Received
September 30, 1987
Decision Date
October 20, 1987
Product Code
KDJ
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
KDJ Set, Administration, For Peritoneal Dialysis, Disposable

Similar 510(k) Clearances

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

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Other Clearances by Travenol Laboratories, S.A.

K Number Device Name
K874181 BAXTER BEDSIDE SYSTEM
K873894 CONTINU-FLO SOLUTION W/CHECK VALVE 2 Y-INJECT SITE
K873873 RESUBMITTED MICRON TRANSFUSION FILTER
K872364 HEMODIALYSIS (SPS), MODEL 550, CODE 5M1309
K872652 UPGRADED AUTO PERITONEAL DIALYSIS CYCLER SYSTEM
K870801 FLO-GARD 6200 VOLUMETRIC INFUSION/PUMPING BLOOD
K871908 IV ADMINISTRATION SET
K871471 CAPILLARY FLOW DIALYZERS MODELS ST-12 & ST-15
K865029 CONTINU-FLO SOLUTION ADMIN. SET W/IN-LINE FILTER
K870169 CAPILLARY FLOW DIALYZERS
Search all 206 clearances from Travenol Laboratories, S.A. →