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

ALPHA TALKER

K Number: K935317 · Decision Mar 28, 1994
Classifications
1
FEI Numbers
125
Registration Numbers
125
Same Product Code
580
Applicant Total
9
Review Days
144

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Basic Information

Device Name
ALPHA TALKER
K Number
K935317
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
890.3860
Medical Specialty
Physical Medicine
Decision
Substantially Equivalent for Some Indications
Applicant
Prentke Romich Co.
Date Received
November 4, 1993
Decision Date
March 28, 1994
Product Code
ITI
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
ITI Wheelchair, Powered

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K925527 LIGHT TALKER
K914259 TOUCH TALKER
K902664 HOSPITAL/HOME ENVIRONMENTAL CONTROL SYST/HECS-1
K902206 CONTROL 1 ENVIRONMENTAL CONTROL