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

ANTICARDIOLIPIN ANTIBODY TEST SYSTEM

K Number: K903531 · Decision Jan 25, 1991
Classifications
1
FEI Numbers
16
Registration Numbers
16
Same Product Code
50
Applicant Total
24
Review Days
172

Basic Information

Device Name
ANTICARDIOLIPIN ANTIBODY TEST SYSTEM
K Number
K903531
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
864.7925
Medical Specialty
Hematology
Decision
Substantially Equivalent
Applicant
MEDICAL INNOVATIONS CORP.
Date Received
August 6, 1990
Decision Date
January 25, 1991
Product Code
GFO
Advisory Committee
Hematology
Review Advisory Committee
IM
Third Party
N

Classifications

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

Product Code Device Name
GFO Activated Partial Thromboplastin

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K943685 MIC DISPOSABLE SNARE
K926581 MIC TRANSGASTRIC JEJUNAL TUBE
K921652 MIC TRANSGASTRIC JEJUNAL FEEDING TUBE KIT
K921370 MIC GASTRO-ENTEROSTOMY TUBE MODIFICATION
K924065 MIC PEG TUBE
K922667 MIC LOW PROFILE GASTROSTOMY TUBE
K913320 MIL CM-II COAGULATION MACHINE
K900464 MIC PERCUTANEOUS ENDOSCOPIC GASTROSTOMY TUBE
Search all 24 clearances from MEDICAL INNOVATIONS CORP. →