FDA 510(k) FDA unclassified Substantially Equivalent 🇺🇸 United States

TACTAID

K Number: K830418 · Decision Mar 10, 1983
Classifications
1
FEI Numbers
0
Registration Numbers
0
Same Product Code
7
Applicant Total
1
Review Days
30

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Basic Information

Device Name
TACTAID
K Number
K830418
Device Class
FDA unclassified
Clearance Type
Traditional
Medical Specialty
Unknown
Decision
Substantially Equivalent
Applicant
Audiological Engineering Corp.
Date Received
February 8, 1983
Decision Date
March 10, 1983
Product Code
LRA
Advisory Committee
Unknown
Review Advisory Committee
EN
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
LRA Hearing Aid, Tactile

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