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

MEDISYSTEMS PERITONEAL DIALYSIS SETS

K Number: K963668 · Decision Aug 15, 1997
Classifications
1
FEI Numbers
24
Registration Numbers
24
Same Product Code
112
Applicant Total
22
Review Days
336

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Basic Information

Device Name
MEDISYSTEMS PERITONEAL DIALYSIS SETS
K Number
K963668
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.5630
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Medisystems Corp.
Date Received
September 13, 1996
Decision Date
August 15, 1997
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

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Other Clearances by Medisystems Corp.

K Number Device Name
K062953 MEDISYSTEMS ARTERIAL-VENOUS FISTULA NEEDLE SET WITH SECUREMENT DEVICE
K010279 MEDISYSTEMS LUER ACCESS INJECTION SITE
K002372 ACCESS ALERT GAUGE
K994306 REVERSO
K990803 MEDISYSTEMS BUTTONHOLE NEEDLE SETS
K983076 MEDISYSTEMS TRANSDUCER PROTECTOR
K971860 MEDISYSTEMS DIALYSIS PRIMING SETS
K970536 MEDISYSTEMS TRANDUCER PROTECTOR
K953823 ARTERIAL VENOUS BLOOD TUBING SET
K932074 MEDISYSTEMS APHERESIS NEEDLE WITH GUARD
Search all 22 clearances from Medisystems Corp. →