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

TH0R DDII IR LAMP SYSTEM

K Number: K033923 · Decision Mar 17, 2004
Classifications
1
FEI Numbers
462
Registration Numbers
462
Same Product Code
228
Applicant Total
2
Review Days
90

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Basic Information

Device Name
TH0R DDII IR LAMP SYSTEM
K Number
K033923
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
890.5500
Medical Specialty
Physical Medicine
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Thor Intl.
Date Received
December 18, 2003
Decision Date
March 17, 2004
Product Code
ILY
Advisory Committee
Physical Medicine
Review Advisory Committee
PM
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
ILY Lamp, Infrared, Therapeutic Heating

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Other Clearances by Thor Intl.

K Number Device Name
K030226 THOR DDII 830CL3 LASER SYSTEM