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

ADFUSE(TM)

K Number: K881590 · Decision May 23, 1988
Classifications
1
FEI Numbers
149
Registration Numbers
149
Same Product Code
847
Applicant Total
9
Review Days
40

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Basic Information

Device Name
ADFUSE(TM)
K Number
K881590
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5725
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Applicant
Healthtek, Inc.
Date Received
April 13, 1988
Decision Date
May 23, 1988
Product Code
FRN
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
FRN Pump, Infusion

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K874495 ADCOMP 4000 HP SYSTEM
K873848 RETROBULBAR NEEDLE
K860610 ADCOMP
K860372 FAST FLOW XX (AQUEOUS SOLUTION FILTER)
K854008 STATLOCK