FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

THERA-CANE

K Number: K903820 · Decision Sep 19, 1990
Classifications
1
FEI Numbers
176
Registration Numbers
176
Same Product Code
12
Applicant Total
1
Review Days
30

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Basic Information

Device Name
THERA-CANE
K Number
K903820
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
890.5660
Medical Specialty
Physical Medicine
Decision
Substantially Equivalent
Applicant
Pro Message Co.
Date Received
August 20, 1990
Decision Date
September 19, 1990
Product Code
LYG
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
LYG Massager, Therapeutic, Manual

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