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

INTRAVASCULAR ADMINISTRATION SET

K Number: K891072 · Decision Apr 21, 1989
Classifications
1
FEI Numbers
424
Registration Numbers
424
Same Product Code
1173
Applicant Total
7
Review Days
51

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Basic Information

Device Name
INTRAVASCULAR ADMINISTRATION SET
K Number
K891072
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5440
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Applicant
Multi-Med, Inc.
Date Received
March 1, 1989
Decision Date
April 21, 1989
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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Other Clearances by Multi-Med, Inc.

K Number Device Name
K890424 ENTERAL FEEDING CONTAINER
K890396 EXTERNAL FEEDING SET FOR PUMP USE
K891176 INJECTION SITE PLUG (INTRAVASCULAR ADMINISTRATION)
K891919 INTRAVASCULAR ADMINISTRATION SET
K890340 INTRAVASCULAR ADMINISTRATION SET
K890127 INTRAVASCULAR ADMINISTRATION SET