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

LUMISCOPE EMS 8000

K Number: K901849 · Decision Aug 24, 1990
Classifications
1
FEI Numbers
170
Registration Numbers
170
Same Product Code
547
Applicant Total
13
Review Days
122

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Basic Information

Device Name
LUMISCOPE EMS 8000
K Number
K901849
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
890.5850
Medical Specialty
Physical Medicine
Decision
Substantially Equivalent
Applicant
Lumiscope Co., Inc.
Date Received
April 24, 1990
Decision Date
August 24, 1990
Product Code
IPF
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
IPF Stimulator, Muscle, Powered

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Other Clearances by Lumiscope Co., Inc.

K Number Device Name
K032714 CARDICARE MODEL MT-301F & MT-301C
K954792 LUMISCOPE MODEL 2018 THERMOMETER
K931768 INTERFERENTIAL CURRENT THERAPY UNIT
K925054 INFRARED LAMP
K924081 LUMISONIC
K920099 GYMMAN
K901096 LUMISCOPE ALTERNATING PRESSURE PAD & PUMP
K901726 LUMISCOPE MICRO 100
K901809 LUMISCOPE ELECTRODES MODELS EL-08,11,15,06,21,25
K894127 LUMISCOPE MODEL 1000/APCC MODEL 1000
Search all 13 clearances from Lumiscope Co., Inc. →