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

DAHLBERG MODEL GF MICROPROCESSOR AUDIOMETER

K Number: K854835 · Decision Mar 4, 1986
Classifications
1
FEI Numbers
62
Registration Numbers
62
Same Product Code
234
Applicant Total
23
Review Days
91

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
DAHLBERG MODEL GF MICROPROCESSOR AUDIOMETER
K Number
K854835
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
874.1050
Medical Specialty
Ear, Nose, Throat
Decision
Substantially Equivalent
Applicant
Miracle-Ear/Dahlberg, Inc.
Date Received
December 3, 1985
Decision Date
March 4, 1986
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 Miracle-Ear/Dahlberg, Inc.

K Number Device Name
K942893 MIRACLE-EAR MODEL PGF + REMOTE
K942895 MIRACLE EAR MODEL PGM
K942894 MIRACLE-EAR MODEL PGC
K941859 MIRACLE-EAR EAR IMPRESSION MATERIAL
K862103 MODEL UC IN-THE-CANAL HEARING AID
K862099 DAHLBERG MODEL EE BEHIND-THE-EAR HEARING AID
K862101 MODEL UM IN-THE-CANAL HEARING AID
K862104 MODEL UC SPECTRUM IN-THE-CANAL HEARING AID
K862102 MODEL KM IN-THE-CANAL HEARING AID
K862100 MODEL ED BEHIND-THE-EAR HEARING AID
Search all 23 clearances from Miracle-Ear/Dahlberg, Inc. →