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

ADVANCE CONTRAST MEDIA SETS (VARYING LENGTH)

K Number: K900187 · Decision May 1, 1990
Classifications
1
FEI Numbers
437
Registration Numbers
437
Same Product Code
1167
Applicant Total
31
Review Days
105

Basic Information

Device Name
ADVANCE CONTRAST MEDIA SETS (VARYING LENGTH)
K Number
K900187
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5440
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Applicant
ADVANCE MEDICAL DESIGNS, INC.
Date Received
January 16, 1990
Decision Date
May 1, 1990
Product Code
FPA
Advisory Committee
General Hospital
Review Advisory Committee
RA
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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