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

BRACHYTHERAPY NEEDLES, RP SLEEVE, RP BRACHY-SPACER, GOLD MAKERS

K Number: K103449 · Decision Feb 25, 2011
Classifications
1
FEI Numbers
35
Registration Numbers
35
Same Product Code
150
Applicant Total
27
Review Days
94

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Basic Information

Device Name
BRACHYTHERAPY NEEDLES, RP SLEEVE, RP BRACHY-SPACER, GOLD MAKERS
K Number
K103449
Device Class
FDA class 2
Clearance Type
Abbreviated
Regulation Number
892.5730
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Riverpoint Medical
Date Received
November 23, 2010
Decision Date
February 25, 2011
Product Code
KXK
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
KXK Source, Brachytherapy, Radionuclide

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