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

BOSCH TOP STAR III

K Number: K820041 · Decision Jan 22, 1982
Classifications
1
FEI Numbers
101
Registration Numbers
101
Same Product Code
1366
Applicant Total
7
Review Days
15

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Basic Information

Device Name
BOSCH TOP STAR III
K Number
K820041
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
874.3300
Medical Specialty
Ear, Nose, Throat
Decision
Substantially Equivalent
Applicant
Bosch Hearing Instruments, Inc.
Date Received
January 7, 1982
Decision Date
January 22, 1982
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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K800779 OMNITON MT80-A BODY HEARING AID