FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

MAICO MA52

K Number: K971080 · Decision Jun 6, 1997
Classifications
1
FEI Numbers
62
Registration Numbers
62
Same Product Code
234
Applicant Total
9
Review Days
73

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Basic Information

Device Name
MAICO MA52
K Number
K971080
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
874.1050
Medical Specialty
Ear, Nose, Throat
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Bernafon-Maico, Inc.
Date Received
March 25, 1997
Decision Date
June 6, 1997
Product Code
EWO
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
EWO Audiometer

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Other Clearances by Bernafon-Maico, Inc.

K Number Device Name
K982723 MAICO MA42
K981142 MAICO MA53
K974211 OPUS 2 - FULL CONCHA SERIES - ITE
K974152 OPUS 2 - COMPLETELY-IN-CANAL SERIES (CIC)
K974069 OPUS 2 - CANAL SERIES (ITC)
K973948 DUALINE 100 BTE
K971158 DUALINE 400 CIC
K962275 MAICO MA25 SERIES II WITH SPEECH