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

SOUND SELECTOR FULL-SERVICE AUDIOMETER

K Number: K933097 · Decision Jan 24, 1994
Classifications
1
FEI Numbers
62
Registration Numbers
62
Same Product Code
234
Applicant Total
2
Review Days
214

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Basic Information

Device Name
SOUND SELECTOR FULL-SERVICE AUDIOMETER
K Number
K933097
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
Ensoniq Corp.
Date Received
June 24, 1993
Decision Date
January 24, 1994
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

Similar 510(k) Clearances

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

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Other Clearances by Ensoniq Corp.

K Number Device Name
K882633 ENSONIQ SOUND SELECTOR, BTE DIGITAL PROG. HRNG AID