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

STARKEY TRILOGY II PROGRAMMABLE HEARING AID

K Number: K933113 · Decision Jul 27, 1993
Classifications
1
FEI Numbers
117
Registration Numbers
117
Same Product Code
1366
Applicant Total
59
Review Days
32

Basic Information

Device Name
STARKEY TRILOGY II PROGRAMMABLE HEARING AID
K Number
K933113
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
STARKEY LABORATORIES, INC.
Date Received
June 25, 1993
Decision Date
July 27, 1993
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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