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

LYRIC2

K Number: K130790 · Decision Jun 27, 2013
Classifications
1
FEI Numbers
101
Registration Numbers
101
Same Product Code
1366
Applicant Total
2
Review Days
97

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Basic Information

Device Name
LYRIC2
K Number
K130790
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
874.3300
Medical Specialty
Ear, Nose, Throat
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Phonak, LLC
Date Received
March 22, 2013
Decision Date
June 27, 2013
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 Phonak, LLC

K Number Device Name
K123450 PHONAK TINNITUS BALANCE