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

DIGITAL FLUORO STORE(DFS) W/NUMERICAL SUFFIXES

K Number: K913012 · Decision Sep 23, 1991
Classifications
1
FEI Numbers
136
Registration Numbers
136
Same Product Code
299
Applicant Total
16
Review Days
77

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Basic Information

Device Name
DIGITAL FLUORO STORE(DFS) W/NUMERICAL SUFFIXES
K Number
K913012
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1650
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Eigen
Date Received
July 8, 1991
Decision Date
September 23, 1991
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

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Other Clearances by Eigen

K Number Device Name
K222222 Artemis, Artemis TPO, Artemis MX
K173744 ProFuse CAD
K162474 Artemis
K063846 EIGEN DSA 2000
K933115 DIGITAL DISK RECORDER
K924164 DIGITAL DISK RECORDER W/DUALPATH ARCHIVE/30-60 OPT
K923585 DIGITAL FLUORO STORE
K905111 DIGITAL DISK RECORDER(DDR) W/NUMERICAL SUFFIXES
K903821 PSC-1 W/OTHER NUMERICAL
K902927 DIGITAL PHOTOSPOT
Search all 16 clearances from Eigen →