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

EZMANAGER MAX DIABETES MANAGEMENT SOFTWARE

K Number: K063674 · Decision Mar 30, 2007
Classifications
1
FEI Numbers
38
Registration Numbers
38
Same Product Code
83
Applicant Total
10
Review Days
109

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Basic Information

Device Name
EZMANAGER MAX DIABETES MANAGEMENT SOFTWARE
K Number
K063674
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5725
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Animas Corp.
Date Received
December 11, 2006
Decision Date
March 30, 2007
Product Code
LZG
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
LZG Pump, Infusion, Insulin

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (LZG), ordered by most recent decision date.

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Other Clearances by Animas Corp.

K Number Device Name
K080639 SYMPHONY GLUCOSE MANAGEMENT SYSTEM
K080587 EZ MANAGER MAX DIABETES MANAGEMENT SOFTWARE
K042873 ANIMAS MODEL IR1250 INSULIN INFUSION PUMP
K032257 MODEL IR 1200 INSULIN PUMP
K022394 EZMANAGER PLUS
K021700 ANIMUS EZSERTER INFUSION SET INSERTER
K021439 MODEL R1000 IR INSULIN PUMP, EZLINK SOFTWARE, SERMON SOFTWARE, R1000 IR DOWNLOAD CRADLE, AND SERIAL INTERFACE ADAPTOR DO
K012754 EZ SET INFUSION SET
K993184 R1000 SERIES INSULIN PUMP