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

NEXUS DRF DIGITAL X-RAY IMAGING SYSTEM

K Number: K103416 · Decision Mar 17, 2011
Classifications
1
FEI Numbers
118
Registration Numbers
118
Same Product Code
319
Applicant Total
14
Review Days
115

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Basic Information

Device Name
NEXUS DRF DIGITAL X-RAY IMAGING SYSTEM
K Number
K103416
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
892.1650
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Infimed, Inc.
Date Received
November 22, 2010
Decision Date
March 17, 2011
Product Code
OWB
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
OWB Interventional Fluoroscopic X-Ray System

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Other Clearances by Infimed, Inc.

K Number Device Name
K112180 I5 DIGITAL X-RAY IMAGING SYSTEM (WITH SDX-4336CP)
K111344 I5 DIGITAL X-RAY IMAGING SYSTEM (WITH FLAATZ 560)
K101833 INFISTITCH FOR I5 DIGITAL X-RAY IMAGING SYSTEM, MODEL I5
K093066 I5 DIGITAL X-RAY IMAGING SYSTEM, MODEL I5
K012490 ORION DIGITAL IMAGING SYSTEM
K992392 RTLX
K992794 STINGRAY DR, MODEL 1
K992575 CARDIOVASCULAR WORKSTATION, MODEL CWS 5000/CWS 3000
K962422 INFIMED DENTAL SYSTEM
K963037 PATRIOT
Search all 14 clearances from Infimed, Inc. →