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

MEDISYSTEMS TRANDUCER PROTECTOR

K Number: K970536 · Decision May 12, 1997
Classifications
1
FEI Numbers
21
Registration Numbers
21
Same Product Code
34
Applicant Total
22
Review Days
89

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Basic Information

Device Name
MEDISYSTEMS TRANDUCER PROTECTOR
K Number
K970536
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
February 12, 1997
Decision Date
May 12, 1997
Product Code
FIB
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
FIB Protector, Transducer, Dialysis

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
K963668 MEDISYSTEMS PERITONEAL DIALYSIS SETS
K953823 ARTERIAL VENOUS BLOOD TUBING SET
K932074 MEDISYSTEMS APHERESIS NEEDLE WITH GUARD
Search all 22 clearances from Medisystems Corp. →