FDA 510(k) FDA class 3 Substantially Equivalent 🇮🇱 Israel

ARTERIAL BLOOD GASSING MONITORING SYSTEM (ABG)

K Number: K870016 · Decision May 28, 1987
Classifications
1
FEI Numbers
24
Registration Numbers
24
Same Product Code
486
Applicant Total
15
Review Days
146

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Basic Information

Device Name
ARTERIAL BLOOD GASSING MONITORING SYSTEM (ABG)
K Number
K870016
Device Class
FDA class 3
Clearance Type
Traditional
Regulation Number
870.3680
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Migada, Ltd.
Date Received
January 2, 1987
Decision Date
May 28, 1987
Product Code
DTB
Advisory Committee
Cardiovascular
Review Advisory Committee
CV
Third Party
N

Classifications

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

Product Code Device Name
DTB Permanent Pacemaker Electrode

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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
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
K860605 FILTER SET 1) 1.2 MIC FILTER 2) 3.0 MIC FILTER
Search all 15 clearances from Migada, Ltd. →