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

ARTISAN PROGRAMMER & HEARING AID

K Number: K935048 · Decision Feb 9, 1994
Classifications
1
FEI Numbers
21
Registration Numbers
21
Same Product Code
23
Applicant Total
50
Review Days
111

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Basic Information

Device Name
ARTISAN PROGRAMMER & HEARING AID
K Number
K935048
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
Telex Communications, Inc.
Date Received
October 21, 1993
Decision Date
February 9, 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

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (LRB), ordered by most recent decision date.

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Other Clearances by Telex Communications, Inc.

K Number Device Name
K984243 TELEX TINNITUS-COMPANION
K982683 TELEX SELECT 1-40 WITH ADAPTIVE COMPRESSION
K964639 TELEX IN-THE-EAR CUSTOM HEARING AID WITH THRESHOLD COMPRESSION-II
K963915 TELEX IN-THE-EAR CUSTOM HEARING AID WITH THRESHOLD COMPRESSION
K961143 TELEX SELECT 2-40 WITH ADAPTIVE COMPRESSION S2-40
K954579 TELEX 349 MULTI CROS W/ADAPIVE COMPRESSION
K943961 THE MODEL ACAPPELLA IN THE EAR HEARING AID
K935366 BINAURAL HEARING AID
K933579 MEMOREX ARTISAN SYSTEM/ARTISAN PROGRAMMER AND CUSTOM HEARING AID
K933095 351-AGCO BEHIND-THE-EAR HEARING AID
Search all 50 clearances from Telex Communications, Inc. →