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

FORTE, MODELS CPS 400 COMBO, CPS 200 COMBO

K Number: K982830 · Decision Nov 6, 1998
Classifications
1
FEI Numbers
19
Registration Numbers
19
Same Product Code
53
Applicant Total
70
Review Days
87

Basic Information

Device Name
FORTE, MODELS CPS 400 COMBO, CPS 200 COMBO
K Number
K982830
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
890.5860
Medical Specialty
Physical Medicine
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
CHATTANOOGA GROUP, INC.
Date Received
August 11, 1998
Decision Date
November 6, 1998
Product Code
IMG
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
IMG Stimulator, Ultrasound And Muscle, For Use In Applying Therapeutic Deep Heat

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Other Clearances by CHATTANOOGA GROUP, INC.

K Number Device Name
K011243 CHATTANOOGA DRY HEAT WHIRLPOOL, MODEL 2000
K982317 VECTRA COMBO
K982324 VECTRA PRO MODELS 2 AND 4
K982321 VECTRA STIM MODELS 200 AND 400
K982829 FORTE, MODEL CPS ULTRASOUND
K982828 FORTE, MODELS CPS 400 STIM, CPS 200 STIM
K980718 PARA-CARE
K974497 INTELECT
K973024 INTELECT LEGEND ULTRASOUND
K972487 EMG RETRAINER
Search all 70 clearances from CHATTANOOGA GROUP, INC. →