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

CLOSED DISCONNECT SYSTEM

K Number: K900106 · Decision Jul 16, 1990
Classifications
1
FEI Numbers
24
Registration Numbers
24
Same Product Code
112
Applicant Total
27
Review Days
188

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Basic Information

Device Name
CLOSED DISCONNECT SYSTEM
K Number
K900106
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.5630
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Applicant
Delmed, Inc.
Date Received
January 9, 1990
Decision Date
July 16, 1990
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 Delmed, Inc.

K Number Device Name
K895142 ENTERAL PUMP SET WITH ENTERAL SPIKE
K895650 ENTERAL PUMP SET W/ENTERA-FLO SPIKE
K895329 600ML AND 1200ML ENTERAL BAG ADM. SET FOR ENTERA
K894506 ENTERA-FLO ENTERAL FEEDING PUMP
K901478 DELMED 80/2 DIALYSIS SYSTEM W/LAST BAG OPTION
K901477 DELMED 80/2 DIALYSIS SYSTEM W/ULTRAFILTRATION
K895246 FRENTA(R) DUO-SET
K895330 600ML AND 1200ML ENTERAL BAG ADM. SET FOR FRENTA
K895919 ENTERAL BAG ADMINI. SETS FOR USE W/FLEXIFLO-III
K895696 ENTERAL PUMP SET W/ENTERAL SPIKE FOR USE W/FEED PU
Search all 27 clearances from Delmed, Inc. →