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

EARETTE HEARING AID SEARS #8054

K Number: K810379 · Decision Mar 4, 1981
Classifications
1
FEI Numbers
106
Registration Numbers
106
Same Product Code
4
Applicant Total
57
Review Days
19

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Basic Information

Device Name
EARETTE HEARING AID SEARS #8054
K Number
K810379
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
880.5160
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Applicant
Oticon Corp.
Date Received
February 13, 1981
Decision Date
March 4, 1981
Product Code
FSD
Advisory Committee
General Hospital
Review Advisory Committee
HO
Third Party
N

Classifications

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

Product Code Device Name
FSD Binder, Abdominal

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Other Clearances by Oticon Corp.

K Number Device Name
K963788 PRIMOFOCUS COMPACT
K932670 OTICON MF
K923490 BTE HEARING AID PERSONIC 410
K923388 BTE HEARING AID OTICON MODEL: MULTIFOCUS POWER
K923491 BTE HEARING AID PERSONIC 425
K905555 A-ZILICONE
K904673 OTICAON BTE MODEL E34P
K902559 CUSTOM IN-THE-EAR HEARING AID OTICON MODEL: P
K902351 CUSTOM ITE HEARING AID MODELS C AND M
K902352 CUSTOM ITE HEARING AID MODEL: H
Search all 57 clearances from Oticon Corp. →