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

PRECISION 500D R&F X-RAY SYSTEM

K Number: K081091 · Decision Jun 11, 2008
Classifications
1
FEI Numbers
136
Registration Numbers
136
Same Product Code
299
Applicant Total
168
Review Days
56

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
PRECISION 500D R&F X-RAY SYSTEM
K Number
K081091
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1650
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
GE Healthcare
Date Received
April 16, 2008
Decision Date
June 11, 2008
Product Code
JAA
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
JAA System, X-Ray, Fluoroscopic, Image-Intensified

Similar 510(k) Clearances

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

View all

Other Clearances by GE Healthcare

K Number Device Name
K253639 View
K242925 MR Contour DL
K232346 Digital Expert Access with Remote Scanning
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
Search all 168 clearances from GE Healthcare →