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

SAGE CONTRAST MANAGEMENT SYSTEM

K Number: K991112 · Decision Sep 2, 1999
Classifications
1
FEI Numbers
424
Registration Numbers
424
Same Product Code
1173
Applicant Total
1
Review Days
154

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Basic Information

Device Name
SAGE CONTRAST MANAGEMENT SYSTEM
K Number
K991112
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5440
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Sage Laboratories, Inc.
Date Received
April 1, 1999
Decision Date
September 2, 1999
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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