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

APERTO Lucent MRI System

K Number: K233629 · Decision May 10, 2024
Classifications
1
FEI Numbers
146
Registration Numbers
146
Same Product Code
1098
Applicant Total
13
Review Days
179

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
APERTO Lucent MRI System
K Number
K233629
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1000
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
FUJIFILM Healthcare Americas Corporation
Date Received
November 13, 2023
Decision Date
May 10, 2024
Product Code
LNH
Advisory Committee
Radiology
Review Advisory Committee
RA
Third Party
N

Classifications

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

Product Code Device Name
LNH System, Nuclear Magnetic Resonance Imaging

Similar 510(k) Clearances

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

View all

Other Clearances by FUJIFILM Healthcare Americas Corporation

K Number Device Name
K261713 Synapse PACS (7.6.0)
K251204 FUJIFILM Stiffening Wire Device (SW-2000)
K243647 Synapse PACS (7.5)
K233321 Double Balloon Endoscope EN-840T, Over-tube TS-1214C
K233687 ECHELON Synergy V10.0
K233583 FCT iSTREAM Phase 1
K240075 FUJIFILM Endoscope Model EB-710XT
K231666 Endoscopic Ultrasonic Probe (P2612S-L); Endoscopic Ultrasonic Probe (P2620S-L)
K231941 ARIETTA x10
K231574 Scenaria View 4.2
Search all 13 clearances from FUJIFILM Healthcare Americas Corporation →