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

CONTRAST CONTROL DEVICE

K Number: K982123 · Decision Jul 21, 1998
Classifications
1
FEI Numbers
437
Registration Numbers
437
Same Product Code
1167
Applicant Total
48
Review Days
35

Basic Information

Device Name
CONTRAST CONTROL DEVICE
K Number
K982123
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5440
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
MEDEX, INC.
Date Received
June 16, 1998
Decision Date
July 21, 1998
Product Code
FPA
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
FPA Set, Administration, Intravascular

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