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

PRESSONE™

K Number: K253047 · Decision Mar 24, 2026
Classifications
1
FEI Numbers
440
Registration Numbers
440
Same Product Code
687
Applicant Total
34
Review Days
183

Basic Information

Device Name
PRESSONE™
K Number
K253047
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5570
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Nipro Medical Corporation
Date Received
September 22, 2025
Decision Date
March 24, 2026
Product Code
FMI
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
FMI Needle, Hypodermic, Single Lumen

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