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

LUMISCOPE ELECTRODES MODELS EL-08,11,15,06,21,25

K Number: K901809 · Decision Jun 18, 1990
Classifications
1
FEI Numbers
243
Registration Numbers
243
Same Product Code
436
Applicant Total
13
Review Days
59

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Basic Information

Device Name
LUMISCOPE ELECTRODES MODELS EL-08,11,15,06,21,25
K Number
K901809
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.1320
Medical Specialty
Neurology
Decision
Substantially Equivalent
Applicant
Lumiscope Co., Inc.
Date Received
April 20, 1990
Decision Date
June 18, 1990
Product Code
GXY
Advisory Committee
Neurology
Review Advisory Committee
NE
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
GXY Electrode, Cutaneous

Similar 510(k) Clearances

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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
K901849 LUMISCOPE EMS 8000
K901096 LUMISCOPE ALTERNATING PRESSURE PAD & PUMP
K901726 LUMISCOPE MICRO 100
K894127 LUMISCOPE MODEL 1000/APCC MODEL 1000
Search all 13 clearances from Lumiscope Co., Inc. →