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

EAR ELECTRODE-ADULT & PEDIATRIC

K Number: K780537 · Decision Jun 2, 1978
Classifications
1
FEI Numbers
243
Registration Numbers
243
Same Product Code
436
Applicant Total
19
Review Days
60

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Basic Information

Device Name
EAR ELECTRODE-ADULT & PEDIATRIC
K Number
K780537
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.1320
Medical Specialty
Neurology
Decision
Substantially Equivalent
Applicant
Life-Tech Instruments, Inc.
Date Received
April 3, 1978
Decision Date
June 2, 1978
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

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Other Clearances by Life-Tech Instruments, Inc.

K Number Device Name
K812177 LIFE-TECH #1857 PRESSURE/POLOT MODULE
K812179 LIFE-TECH #1753 BIOFEEDBACK TRAINER
K812180 LIFE-TECH #5102 VISULAB
K812178 LIFE-TECH #'S 1106/1156 UROLABS
K800112 AMBLYOPIA TRAINER
K790663 MODEL 1750 STANDING URINAL
K790664 MODEL 1309 AUDIO MONITOR
K781476 MULAR GOLD LEAF ELECTRODE MODEL 7501
K781461 MODEL 7320 VISUAL STIMULATOR
K781475 ELECTRODE IMPEDANCE TESTER-MODEL 500
Search all 19 clearances from Life-Tech Instruments, Inc. →