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

MUL-T-PAD

K Number: K832819 · Decision Sep 26, 1983
Classifications
1
FEI Numbers
123
Registration Numbers
123
Same Product Code
92
Applicant Total
27
Review Days
38

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Basic Information

Device Name
MUL-T-PAD
K Number
K832819
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
890.5720
Medical Specialty
Physical Medicine
Decision
Substantially Equivalent
Applicant
Gaymar Industries, Inc.
Date Received
August 19, 1983
Decision Date
September 26, 1983
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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K961854 SPR PLUS II OVERLAY SYSTEM (CL250/CL212
K942881 TC 3000
K930345 TC2000 POWER UNIT AND ACCESSORIES
K914921 SCM-3 AND ACCESSORIES
K914805 TC-1000, TC-1050 SYSTEM
K914851 CLA-1400 SYSTEM
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