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

EARETTE HEARING AID(BEHING THE EAR)

K Number: K810576 · Decision Mar 17, 1981
Classifications
1
FEI Numbers
117
Registration Numbers
117
Same Product Code
1366
Applicant Total
57
Review Days
14

Basic Information

Device Name
EARETTE HEARING AID(BEHING THE EAR)
K Number
K810576
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
874.3300
Medical Specialty
Ear, Nose, Throat
Decision
Substantially Equivalent
Applicant
OTICON CORP.
Date Received
March 3, 1981
Decision Date
March 17, 1981
Product Code
ESD
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
ESD Hearing Aid, Air-Conduction, Prescription

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Other Clearances by OTICON CORP.

K Number Device Name
K963788 PRIMOFOCUS COMPACT
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K923388 BTE HEARING AID OTICON MODEL: MULTIFOCUS POWER
K923490 BTE HEARING AID PERSONIC 410
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. →