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

VERT-X

K Number: K061873 · Decision Aug 18, 2006
Classifications
1
FEI Numbers
68
Registration Numbers
68
Same Product Code
81
Applicant Total
22
Review Days
46

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Basic Information

Device Name
VERT-X
K Number
K061873
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1650
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Direx Systems Corp.
Date Received
July 3, 2006
Decision Date
August 18, 2006
Product Code
OXO
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
OXO Image-Intensified Fluoroscopic X-Ray System, Mobile

Similar 510(k) Clearances

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

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Other Clearances by Direx Systems Corp.

K Number Device Name
K111947 DUET MAGNA
K102765 PRONEX
K072529 TRACKPORT
K071701 TRACKLEAF-10
K063482 CROSSPLAN / ACCUSOFT-XL V.4.04
K062147 INTEGRA SL
K062032 ACCUSOFT, ACCUSOFT XL
K061713 MAGIS1;MAGIS2
K052212 MIGUE
K053640 INTEGRA
Search all 22 clearances from Direx Systems Corp. →