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

I.V. ADMINISTRATION SET

K Number: K811837 · Decision Jul 10, 1981
Classifications
1
FEI Numbers
424
Registration Numbers
424
Same Product Code
1173
Applicant Total
22
Review Days
9

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Basic Information

Device Name
I.V. ADMINISTRATION SET
K Number
K811837
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5440
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Applicant
Medisystems Corp.
Date Received
July 1, 1981
Decision Date
July 10, 1981
Product Code
FPA
Advisory Committee
General Hospital
Review Advisory Committee
HO
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
FPA Set, Administration, Intravascular

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K062953 MEDISYSTEMS ARTERIAL-VENOUS FISTULA NEEDLE SET WITH SECUREMENT DEVICE
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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. →