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

LSI6000 THERMAL THERAPY SYSTEM

K Number: K926151 · Decision May 26, 1993
Classifications
1
FEI Numbers
123
Registration Numbers
123
Same Product Code
92
Applicant Total
7
Review Days
170

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Basic Information

Device Name
LSI6000 THERMAL THERAPY SYSTEM
K Number
K926151
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
890.5720
Medical Specialty
Physical Medicine
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Burke Neutech, Inc.
Date Received
December 7, 1992
Decision Date
May 26, 1993
Product Code
ILO
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
ILO Pack, Hot Or Cold, Water Circulating

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Other Clearances by Burke Neutech, Inc.

K Number Device Name
K955326 SPORTS CONTRAST THERAPY SYSTEM ST 7000
K952117 EPILATOR
K943497 CONTRAST 7000 THERAPY SYSTEM
K945803 THERMAFLEX, MODEL SD 55 C.P.M.H.
K942926 NEURO-AIDE
K940160 TS1000 PORTABLE DISPOSABLE COLD THERAPY SYSTEM