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

DIPRIVAN LUER CONNECTOR

K Number: K935274 · Decision Mar 15, 1994
Classifications
1
FEI Numbers
177
Registration Numbers
177
Same Product Code
205
Applicant Total
120
Review Days
132

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Basic Information

Device Name
DIPRIVAN LUER CONNECTOR
K Number
K935274
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5440
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Ohmeda Medical
Date Received
November 3, 1993
Decision Date
March 15, 1994
Product Code
LHI
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
LHI Set, I.V. Fluid Transfer

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