FDA 510(k) FDA class 2 Substantially Equivalent 🇯🇵 Japan

Pen Injector Needle 32.5

K Number: K250700 · Decision Nov 21, 2025
Classifications
1
FEI Numbers
440
Registration Numbers
440
Same Product Code
687
Applicant Total
13
Review Days
259

Basic Information

Device Name
Pen Injector Needle 32.5
K Number
K250700
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5570
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Terumo Corporation
Date Received
March 7, 2025
Decision Date
November 21, 2025
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

Similar 510(k) Clearances

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

View all

Other Clearances by Terumo Corporation

K Number Device Name
K252295 Ryurei
K250751 DualView Catheter
K240818 R2P Radifocus Glidewire Advantage
K240859 Glidewire GT-R
K190427 Immucise
K181369 Immucise Intradermal Injection System
K173799 NaviCross 0.018
K170417 Glidewire GT
K130280 CAPIOX FX HOLLOW FIBER OXYGENATOR W/ RESERVOIR
K130493 CAPIOX RX05 HOLLOW FIBER OXYGENATOR/RESERVOIR
Search all 13 clearances from Terumo Corporation →