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

MEDISYSTEMS BUTTONHOLE NEEDLE SETS

K Number: K990803 · Decision Jan 6, 2000
Classifications
1
FEI Numbers
18
Registration Numbers
18
Same Product Code
78
Applicant Total
22
Review Days
302

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Basic Information

Device Name
MEDISYSTEMS BUTTONHOLE NEEDLE SETS
K Number
K990803
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.5540
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Medisystems Corp.
Date Received
March 10, 1999
Decision Date
January 6, 2000
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

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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
K983076 MEDISYSTEMS TRANSDUCER PROTECTOR
K971860 MEDISYSTEMS DIALYSIS PRIMING SETS
K963668 MEDISYSTEMS PERITONEAL DIALYSIS SETS
K970536 MEDISYSTEMS TRANDUCER PROTECTOR
K953823 ARTERIAL VENOUS BLOOD TUBING SET
K932074 MEDISYSTEMS APHERESIS NEEDLE WITH GUARD
Search all 22 clearances from Medisystems Corp. →