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

REPLACEMENT PUMP HEAD DOOR ASSEMBLY, P1, MODEL BX10468, REPLACEMENT PUMP HEAD DOOR ASSEMBLY, P2, MODEL BX10469

K Number: K032789 · Decision Oct 9, 2003
Classifications
1
FEI Numbers
159
Registration Numbers
159
Same Product Code
844
Applicant Total
7
Review Days
31

Basic Information

Device Name
REPLACEMENT PUMP HEAD DOOR ASSEMBLY, P1, MODEL BX10468, REPLACEMENT PUMP HEAD DOOR ASSEMBLY, P2, MODEL BX10469
K Number
K032789
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5725
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
AMERICAN I.V. PRODUCTS, INC.
Date Received
September 8, 2003
Decision Date
October 9, 2003
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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