FDA 510(k) FDA class 2 Substantially Equivalent 🇮🇱 Israel

MULTISET 40

K Number: K853386 · Decision Aug 22, 1985
Classifications
1
FEI Numbers
28
Registration Numbers
28
Same Product Code
29
Applicant Total
15
Review Days
10

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Basic Information

Device Name
MULTISET 40
K Number
K853386
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5440
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Applicant
Migada, Ltd.
Date Received
August 12, 1985
Decision Date
August 22, 1985
Product Code
BRZ
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
BRZ Set, Blood Transfusion

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Other Clearances by Migada, Ltd.

K Number Device Name
K943095 IV TRANSFER SPIKE
K933929 LAB-SITE(R) SAFETY CANNULA
K902881 LAB-SITE SAFETY NEEDLE
K870016 ARTERIAL BLOOD GASSING MONITORING SYSTEM (ABG)
K864453 EMERGENCY & MILITARY INFUSION SYSTEM
K863304 PRESELECTED FLOW RATE I.V. SET
K860952 I.V. SET WITH AND WITHOUT AIR VENT
K861275 HIGH FLOW I.V. SET
K860595 TRANSFER SET
K854365 IV SETS WITH NO PHTHALATE PLASTICIZER COMPONENTS
Search all 15 clearances from Migada, Ltd. →