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

MULTIDOS, QC6PLUS

K Number: K972211 · Decision Sep 10, 1997
Classifications
1
FEI Numbers
27
Registration Numbers
27
Same Product Code
91
Applicant Total
8
Review Days
90

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Basic Information

Device Name
MULTIDOS, QC6PLUS
K Number
K972211
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.5050
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Ptw-New York Corp.
Date Received
June 12, 1997
Decision Date
September 10, 1997
Product Code
LHN
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
LHN System, Radiation Therapy, Charged-Particle, Medical

Similar 510(k) Clearances

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Other Clearances by Ptw-New York Corp.

K Number Device Name
K062817 PTW DAVID IMRT QC VERIFICATION SYSTEM
K010705 OPTIDOS
K010916 PTW DOSIMETRY DIODE, T60008
K972212 0.015CC PINPOINT IONIZATION CHAMBER, 0.005 CC PINPOINT IONIZATION CHAMBER
K961208 0.6CC IONIZATION CHAMBER - WATERPROOF 0.6CC IONIZATION CHAMBER
K954165 PTW-MP3 & PTW-MP3S AUTOMATIC WATER PHANTOM
K951764 UNIDOS UNIVERSAL DOSIMETER MODEL 10002-WITH TNC CONNECTOR, 10005-WITH BNT CONNECTOR