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

INFRARED LAMP

K Number: K925054 · Decision Jun 29, 1993
Classifications
1
FEI Numbers
462
Registration Numbers
462
Same Product Code
228
Applicant Total
13
Review Days
266

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Basic Information

Device Name
INFRARED LAMP
K Number
K925054
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
890.5500
Medical Specialty
Physical Medicine
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Lumiscope Co., Inc.
Date Received
October 6, 1992
Decision Date
June 29, 1993
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 Lumiscope Co., Inc.

K Number Device Name
K032714 CARDICARE MODEL MT-301F & MT-301C
K954792 LUMISCOPE MODEL 2018 THERMOMETER
K931768 INTERFERENTIAL CURRENT THERAPY UNIT
K924081 LUMISONIC
K920099 GYMMAN
K901849 LUMISCOPE EMS 8000
K901096 LUMISCOPE ALTERNATING PRESSURE PAD & PUMP
K901726 LUMISCOPE MICRO 100
K901809 LUMISCOPE ELECTRODES MODELS EL-08,11,15,06,21,25
K894127 LUMISCOPE MODEL 1000/APCC MODEL 1000
Search all 13 clearances from Lumiscope Co., Inc. →