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

PRE-WAXED NEEDLES WITH GOLD FIDUCIARY MARKERS

K Number: K071550 · Decision Jul 18, 2007
Classifications
1
FEI Numbers
35
Registration Numbers
35
Same Product Code
150
Applicant Total
31
Review Days
42

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Basic Information

Device Name
PRE-WAXED NEEDLES WITH GOLD FIDUCIARY MARKERS
K Number
K071550
Device Class
FDA class 2
Clearance Type
Abbreviated
Regulation Number
892.5730
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Cp Medical
Date Received
June 6, 2007
Decision Date
July 18, 2007
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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Other Clearances by Cp Medical

K Number Device Name
K094028 CP-FIBER (ORTHOFIBER)
K072229 MONOSWIFT
K060987 OSCERA7 SYNTHETIC ABSORBABLE BONE WAX, MODEL OS31
K041894 ORTHOFIBER
K034062 CP SLEEVE AND RIVER SLEEVE
K024372 CP MEDICAL BONE WAX
K030786 MONO-SWIFT
K030351 STAINLESS STEEL SURGICAL SUTURE, NON-ABSORBABLE
K023710 VISORB SWIFT
K022075 DISPOSABLE TEMPORARY PACING CABLE,MODELS CPW-BV-5,CPW-LG-5,CPW-SM-5,CPW-ERA300-5,CPW-QLOC-5
Search all 31 clearances from Cp Medical →