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

ASL CUSTOM IN-THE-EAR HEARING AID #L

K Number: K801023 · Decision May 28, 1980
Classifications
1
FEI Numbers
101
Registration Numbers
101
Same Product Code
1366
Applicant Total
1
Review Days
27

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Basic Information

Device Name
ASL CUSTOM IN-THE-EAR HEARING AID #L
K Number
K801023
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
874.3300
Medical Specialty
Ear, Nose, Throat
Decision
Substantially Equivalent
Applicant
American Sound Labs
Date Received
May 1, 1980
Decision Date
May 28, 1980
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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