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

Digital Expert Access with Remote Scanning

K Number: K232346 · Decision Oct 27, 2023
Classifications
1
FEI Numbers
146
Registration Numbers
146
Same Product Code
1098
Applicant Total
168
Review Days
84

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
Digital Expert Access with Remote Scanning
K Number
K232346
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1000
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
GE Healthcare
Date Received
August 4, 2023
Decision Date
October 27, 2023
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 GE Healthcare

K Number Device Name
K253639 View
K242925 MR Contour DL
K223212 Precision DL
K221680 Xeleris V Processing and Review System
K221932 Omni Legend
K213689 Voluson P6, Voluson P8
K213642 Voluson S6, Voluson S8, Voluson S8t, Voluson S10, Voluson S10 Expert
K211488 LOGIQ E10
K211524 LOGIQ E10s, LOGIQ Fortis
K212004 MyoSPECT, MyoSpect ES
Search all 168 clearances from GE Healthcare →