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

MEDISYSTEMS HEMODIALYSIS FISTULA SET

K Number: K910734 · Decision Jun 20, 1991
Classifications
1
FEI Numbers
18
Registration Numbers
18
Same Product Code
78
Applicant Total
22
Review Days
119

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Basic Information

Device Name
MEDISYSTEMS HEMODIALYSIS FISTULA SET
K Number
K910734
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.5540
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Applicant
Medisystems Corp.
Date Received
February 21, 1991
Decision Date
June 20, 1991
Product Code
FIE
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
FIE Needle, Fistula

Similar 510(k) Clearances

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

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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
K963668 MEDISYSTEMS PERITONEAL DIALYSIS SETS
K970536 MEDISYSTEMS TRANDUCER PROTECTOR
K953823 ARTERIAL VENOUS BLOOD TUBING SET
Search all 22 clearances from Medisystems Corp. →