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

Sparta Infusion Set for Insulin

K Number: K243841 · Decision Aug 1, 2025
Classifications
1
FEI Numbers
424
Registration Numbers
424
Same Product Code
1173
Applicant Total
13
Review Days
231

Basic Information

Device Name
Sparta Infusion Set for Insulin
K Number
K243841
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5440
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Deka Research and Development
Date Received
December 13, 2024
Decision Date
August 1, 2025
Product Code
FPA
Advisory Committee
General Hospital
Review Advisory Committee
CH
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
FPA Set, Administration, Intravascular

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