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

CRC 15ULTRA

K Number: K052595 · Decision Nov 8, 2005
Classifications
1
FEI Numbers
46
Registration Numbers
46
Same Product Code
206
Applicant Total
14
Review Days
48

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Basic Information

Device Name
CRC 15ULTRA
K Number
K052595
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.5700
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Capintec, Inc.
Date Received
September 21, 2005
Decision Date
November 8, 2005
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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K071396 CRC 25 SERIES (CRC 25R, CRC 25PET, CRC 25W) DOSE CALIBRATORS
K030175 2 BASIC
K020150 CRC-15BT
K982448 CARDIOLIGHT
K980402 CAPINTEC MODEL 292 ELECTROMETER
K946387 CAPRA (CAPRAC-R) WIPETEST AND WELL COUNTER
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