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

CAPD U.V. GERMICIDAL CONNECTION SYSTEM

K Number: K812802 · Decision Mar 2, 1982
Classifications
1
FEI Numbers
24
Registration Numbers
24
Same Product Code
112
Applicant Total
206
Review Days
147

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Basic Information

Device Name
CAPD U.V. GERMICIDAL CONNECTION SYSTEM
K Number
K812802
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
October 6, 1981
Decision Date
March 2, 1982
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
K873984 AUTOMATIC PERITONEAL DIALYSIS CYCLER SET (5C4437)
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
Search all 206 clearances from Travenol Laboratories, S.A. →