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

NU.EAR SD-3 IN THE CANAL (ITC) HEARING AID

K Number: K935331 · Decision Jan 21, 1994
Classifications
1
FEI Numbers
101
Registration Numbers
101
Same Product Code
1366
Applicant Total
10
Review Days
77

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Basic Information

Device Name
NU.EAR SD-3 IN THE CANAL (ITC) HEARING AID
K Number
K935331
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
Nu-Ear Electronics
Date Received
November 5, 1993
Decision Date
January 21, 1994
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

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (ESD), ordered by most recent decision date.

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Other Clearances by Nu-Ear Electronics

K Number Device Name
K935328 NU.EAR SS-2 IN THE CANAL (ITC) HEARING AID
K935335 NU.EAR SS-10 IN THE CANAL (ITC) HEARING AID
K935329 NU.EAR AE-2 IN THE CANAL (ITC) HEARING AID
K935327 NU.EAR SD-2 IN-THE-CANAL (ITC) HEARING AID
K935333 NU.EAR SS-1 IN THE EAR (ITE) HEARING AID
K935334 NU.EAR SD-1 IN THE EAR (ITE) HEARING AID
K935332 NU.EAR AE-1 IN THE EAR (ITE) HEARING AID
K935330 NU.EAR SS-3 IN THE CANAL (ITC) HEARING AID
K935326 NU-EAR SD-10 IN THE CANAL HEARING AID