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

LAB-SITE(R) SAFETY CANNULA

K Number: K933929 · Decision Dec 7, 1993
Classifications
1
FEI Numbers
18
Registration Numbers
18
Same Product Code
68
Applicant Total
15
Review Days
119

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Basic Information

Device Name
LAB-SITE(R) SAFETY CANNULA
K Number
K933929
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.5470
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Migada, Ltd.
Date Received
August 10, 1993
Decision Date
December 7, 1993
Product Code
CBF
Advisory Committee
Anesthesiology
Review Advisory Committee
AN
Third Party
N

Classifications

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

Product Code Device Name
CBF Chamber, Hyperbaric

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Other Clearances by Migada, Ltd.

K Number Device Name
K943095 IV TRANSFER SPIKE
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
K860605 FILTER SET 1) 1.2 MIC FILTER 2) 3.0 MIC FILTER
Search all 15 clearances from Migada, Ltd. →