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

ACOUSTIC APPRAISE CD-3

K Number: K923013 · Decision Aug 14, 1992
Classifications
1
FEI Numbers
62
Registration Numbers
62
Same Product Code
234
Applicant Total
39
Review Days
53

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Basic Information

Device Name
ACOUSTIC APPRAISE CD-3
K Number
K923013
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
874.1050
Medical Specialty
Ear, Nose, Throat
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Qualitone
Date Received
June 22, 1992
Decision Date
August 14, 1992
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 Qualitone

K Number Device Name
K961827 IN-THE-EAR
K955466 DYNAMEQ-II OPTION
K955359 CYBER III OPTION UM, UC312, UC10, UCIC
K953884 PROPHET
K935348 ODYSSEY CLINICAL AUDIOMETER
K935289 PRO FIT-CYBER II OPTION
K923006 AS-90
K923007 AT-2
K923986 CYBERNETIC OPTION (CYBER I)
K914017 UC312, ULTRA MINIATURE ITC HEARING AID
Search all 39 clearances from Qualitone →