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

DELTATALKER WITH INFRARED

K Number: K961306 · Decision Jun 27, 1996
Classifications
1
FEI Numbers
17
Registration Numbers
17
Same Product Code
23
Applicant Total
9
Review Days
84

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Basic Information

Device Name
DELTATALKER WITH INFRARED
K Number
K961306
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
890.3725
Medical Specialty
Physical Medicine
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Prentke Romich Co.
Date Received
April 4, 1996
Decision Date
June 27, 1996
Product Code
IQA
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
IQA System, Environmental Control, Powered

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Other Clearances by Prentke Romich Co.

K Number Device Name
K944585 SCANNING DIRECTOR
K933207 WALKERTALKER
K935317 ALPHA TALKER
K925387 LIBERATOR
K925527 LIGHT TALKER
K914259 TOUCH TALKER
K902664 HOSPITAL/HOME ENVIRONMENTAL CONTROL SYST/HECS-1
K902206 CONTROL 1 ENVIRONMENTAL CONTROL