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

EEG TELEPHONE TRANSMITTER, MODEL #T-7

K Number: K813010 · Decision Nov 16, 1981
Classifications
1
FEI Numbers
0
Registration Numbers
0
Same Product Code
19
Applicant Total
14
Review Days
20

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Basic Information

Device Name
EEG TELEPHONE TRANSMITTER, MODEL #T-7
K Number
K813010
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.1855
Medical Specialty
Neurology
Decision
Substantially Equivalent
Applicant
Pharmaquest Corp.
Date Received
October 27, 1981
Decision Date
November 16, 1981
Product Code
GYE
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
GYE Encephalogram Telemetry System

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K833236 TELEPHONE TRANSMITTER T-10 EEG
K833880 TELEPHONIC RECEIVER R-10 EEG
K830705 MINI LANCET-BLOOD LANCET
K822976 HYPOCOUNT A
K822486 HOME BLOOD GLUCOSE MONITOR
K820248 RODDER VOLUME VENTILATOR
K812849 PTT-200 TELEPHONIC PULMONARY TRANSMITT
K812850 PTT-200 PULMONARY RECEIVER/MICROPROCES
K812683 NEONATE FLEXFLOAT
Search all 14 clearances from Pharmaquest Corp. →