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

AUTOFUSER AMBULATORY INFUSION PUMP

K Number: K041585 · Decision Aug 26, 2004
Classifications
1
FEI Numbers
24
Registration Numbers
24
Same Product Code
87
Applicant Total
1
Review Days
73

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Basic Information

Device Name
AUTOFUSER AMBULATORY INFUSION PUMP
K Number
K041585
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5725
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Algos, LC
Date Received
June 14, 2004
Decision Date
August 26, 2004
Product Code
MEB
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
MEB Pump, Infusion, Elastomeric

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