FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

MODULE PROGRAM

K Number: K942722 · Decision Sep 6, 1994
Classifications
1
FEI Numbers
21
Registration Numbers
21
Same Product Code
23
Applicant Total
73
Review Days
89

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Basic Information

Device Name
MODULE PROGRAM
K Number
K942722
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
874.3300
Medical Specialty
Ear, Nose, Throat
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Electone, Inc.
Date Received
June 9, 1994
Decision Date
September 6, 1994
Product Code
LRB
Advisory Committee
Ear, Nose, Throat
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
LRB Face Plate Hearing Aid

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Other Clearances by Electone, Inc.

K Number Device Name
K973266 Z DEQ-II
K961084 AM 400
K955702 SONATA U-01
K953050 Z33
K953047 Z20
K953053 AM 260 PP
K953052 AM 260 K-AMP
K953054 AM 260 OHM
K953051 Z35
K953048 Z22
Search all 73 clearances from Electone, Inc. →