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

EM PROBE, EM PAD

K Number: K024361 · Decision Oct 9, 2003
Classifications
1
FEI Numbers
462
Registration Numbers
462
Same Product Code
228
Applicant Total
1
Review Days
283

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Basic Information

Device Name
EM PROBE, EM PAD
K Number
K024361
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
890.5500
Medical Specialty
Physical Medicine
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Em Probe, Inc.
Date Received
December 30, 2002
Decision Date
October 9, 2003
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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