FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

ELECTRODE IMPEDANCE TESTER-MODEL 500

K Number: K781475 · Decision Sep 7, 1978
Classifications
1
FEI Numbers
8
Registration Numbers
8
Same Product Code
4
Applicant Total
19
Review Days
10

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
ELECTRODE IMPEDANCE TESTER-MODEL 500
K Number
K781475
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
882.1410
Medical Specialty
Neurology
Decision
Substantially Equivalent
Applicant
Life-Tech Instruments, Inc.
Date Received
August 28, 1978
Decision Date
September 7, 1978
Product Code
GYA
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
GYA Tester, Electrode/Lead, Electroencephalograph

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (GYA), ordered by most recent decision date.

View all

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
K781474 PREAMPLIFIER MODELS 8101PI & 8102PI
Search all 19 clearances from Life-Tech Instruments, Inc. →