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

DSP SCREENING AUDIOMETER

K Number: K924543 · Decision Feb 26, 1993
Classifications
1
FEI Numbers
62
Registration Numbers
62
Same Product Code
234
Applicant Total
6
Review Days
171

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
DSP SCREENING AUDIOMETER
K Number
K924543
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
Micro Audiometrics Corp.
Date Received
September 8, 1992
Decision Date
February 26, 1993
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.

View all

Other Clearances by Micro Audiometrics Corp.

K Number Device Name
K982878 EARSCAN 3
K913589 EARSCAN DSP-1 PURE TONE AUDIOMETER
K904270 BIOLINK AUDIOMETER SOFTWARE ACCESSORY
K883505 BIOMETER AUDIOMETER
K812529 EARSCAN