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

FAST FLOW XX (AQUEOUS SOLUTION FILTER)

K Number: K860372 · Decision May 30, 1986
Classifications
1
FEI Numbers
50
Registration Numbers
50
Same Product Code
97
Applicant Total
9
Review Days
116

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Basic Information

Device Name
FAST FLOW XX (AQUEOUS SOLUTION FILTER)
K Number
K860372
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5440
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Applicant
Healthtek, Inc.
Date Received
February 3, 1986
Decision Date
May 30, 1986
Product Code
FPB
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
FPB Filter, Infusion Line

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K Number Device Name
K923448 EMPTY SOLUTION TRANSFER CONTAINER W/ DETACH LEG
K913985 TRANSFER-AID(TM)
K913608 SNAPPER
K881590 ADFUSE(TM)
K874495 ADCOMP 4000 HP SYSTEM
K873848 RETROBULBAR NEEDLE
K860610 ADCOMP
K854008 STATLOCK