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

STOPCOCK & LUER LOCK PLUG

K Number: K954970 · Decision Apr 22, 1996
Classifications
1
FEI Numbers
88
Registration Numbers
88
Same Product Code
88
Applicant Total
48
Review Days
175

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Basic Information

Device Name
STOPCOCK & LUER LOCK PLUG
K Number
K954970
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
October 30, 1995
Decision Date
April 22, 1996
Product Code
FMG
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
FMG Stopcock, I.V. Set

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