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

DAHLBERG MODEL JMS IN-THE-EAR HEARING INSTRUMENT

K Number: K900692 · Decision Mar 14, 1990
Classifications
1
FEI Numbers
117
Registration Numbers
117
Same Product Code
1366
Applicant Total
65
Review Days
29

Basic Information

Device Name
DAHLBERG MODEL JMS IN-THE-EAR HEARING INSTRUMENT
K Number
K900692
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
874.3300
Medical Specialty
Ear, Nose, Throat
Decision
Substantially Equivalent
Applicant
MIRACLE-EAR, INC.
Date Received
February 13, 1990
Decision Date
March 14, 1990
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

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Other Clearances by MIRACLE-EAR, INC.

K Number Device Name
K972345 DAHLBERG/MIRACLE-EAR
K972346 MIRACLE-EAR ITE DIGITAL
K972344 MIRACLE-EAR DIGITAL BTE
K970262 MULTI-CHANNEL COMPRESSION BTE (SD)
K964419 MIRACLE - EAR (ITE/ITC/CIC)
K965057 AUDIOTONE (A554H)
K965063 AUDIOTONE (A-552)
K965049 DAHLBERG (A-554)
K964669 MIRACLE-EAR OR AUDIOTONE
K964794 DAHLBERG K-AMP BTE
Search all 65 clearances from MIRACLE-EAR, INC. →