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

STIMULATOR, SONIC CONTROL (AS-1)

K Number: K760166 · Decision Jul 20, 1976
Classifications
1
FEI Numbers
1
Registration Numbers
1
Same Product Code
5
Applicant Total
7
Review Days
14

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Basic Information

Device Name
STIMULATOR, SONIC CONTROL (AS-1)
K Number
K760166
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.5235
Medical Specialty
Neurology
Decision
Substantially Equivalent
Applicant
Farrall Instruments, Inc.
Date Received
July 6, 1976
Decision Date
July 20, 1976
Product Code
HCB
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
HCB Device, Aversive Conditioning

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