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

INTERSTITIAL NEEDLES

K Number: K073133 · Decision Nov 16, 2007
Classifications
1
FEI Numbers
45
Registration Numbers
45
Same Product Code
203
Applicant Total
85
Review Days
9

Basic Information

Device Name
INTERSTITIAL NEEDLES
K Number
K073133
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
892.5700
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
VARIAN MEDICAL SYSTEMS, INC.
Date Received
November 7, 2007
Decision Date
November 16, 2007
Product Code
JAQ
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
JAQ System, Applicator, Radionuclide, Remote-Controlled

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