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

TOUCH TALKER

K Number: K914259 · Decision Feb 27, 1992
Classifications
1
FEI Numbers
45
Registration Numbers
45
Same Product Code
37
Applicant Total
9
Review Days
157

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Basic Information

Device Name
TOUCH TALKER
K Number
K914259
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
890.3710
Medical Specialty
Physical Medicine
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Prentke Romich Co.
Date Received
September 23, 1991
Decision Date
February 27, 1992
Product Code
ILQ
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
ILQ System, Communication, Powered

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K Number Device Name
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K944585 SCANNING DIRECTOR
K933207 WALKERTALKER
K935317 ALPHA TALKER
K925387 LIBERATOR
K925527 LIGHT TALKER
K902664 HOSPITAL/HOME ENVIRONMENTAL CONTROL SYST/HECS-1
K902206 CONTROL 1 ENVIRONMENTAL CONTROL