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

NaviCross 0.018

K Number: K173799 · Decision Mar 29, 2018
Classifications
1
FEI Numbers
276
Registration Numbers
277
Same Product Code
889
Applicant Total
13
Review Days
105

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
NaviCross 0.018
K Number
K173799
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.1250
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Terumo Corporation
Date Received
December 14, 2017
Decision Date
March 29, 2018
Product Code
DQY
Advisory Committee
Cardiovascular
Review Advisory Committee
CV
Third Party
N

Classifications

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

Product Code Device Name
DQY Catheter, Percutaneous

Similar 510(k) Clearances

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

View all

Other Clearances by Terumo Corporation

K Number Device Name
K252295 Ryurei
K250700 Pen Injector Needle 32.5
K250751 DualView Catheter
K240818 R2P Radifocus Glidewire Advantage
K240859 Glidewire GT-R
K190427 Immucise
K181369 Immucise Intradermal Injection System
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 →