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

ARTERIAL VENOUS BLOOD TUBING SET

K Number: K953823 · Decision Sep 23, 1996
Classifications
1
FEI Numbers
65
Registration Numbers
65
Same Product Code
76
Applicant Total
22
Review Days
405

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Basic Information

Device Name
ARTERIAL VENOUS BLOOD TUBING SET
K Number
K953823
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.5820
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Medisystems Corp.
Date Received
August 15, 1995
Decision Date
September 23, 1996
Product Code
FJK
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
FJK Set, Tubing, Blood, With And Without Anti-Regurgitation Valve

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K990803 MEDISYSTEMS BUTTONHOLE NEEDLE SETS
K983076 MEDISYSTEMS TRANSDUCER PROTECTOR
K971860 MEDISYSTEMS DIALYSIS PRIMING SETS
K963668 MEDISYSTEMS PERITONEAL DIALYSIS SETS
K970536 MEDISYSTEMS TRANDUCER PROTECTOR
K932074 MEDISYSTEMS APHERESIS NEEDLE WITH GUARD
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