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

FLOW EASE(PLASTIC VENTED NEEDLE)

K Number: K853212 · Decision Sep 19, 1985
Classifications
1
FEI Numbers
176
Registration Numbers
176
Same Product Code
200
Applicant Total
17
Review Days
50

Basic Information

Device Name
FLOW EASE(PLASTIC VENTED NEEDLE)
K Number
K853212
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5440
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Applicant
ACACIA, INC.
Date Received
July 31, 1985
Decision Date
September 19, 1985
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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