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

SIBELMED AC50D

K Number: K973377 · Decision Mar 10, 1998
Classifications
1
FEI Numbers
62
Registration Numbers
62
Same Product Code
234
Applicant Total
5
Review Days
183

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Basic Information

Device Name
SIBELMED AC50D
K Number
K973377
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
Trutone
Date Received
September 8, 1997
Decision Date
March 10, 1998
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 Trutone

K Number Device Name
K972550 AUDIFON H24 AGC/AUDIFON H25 AGC/AUDIFON H30 AGC
K972552 AUDIFON H20 PC/AUDIFON H32 PP
K972542 JAZZ PP AGC-O, JAZZ PP
K972543 TWIST PPAGC-1, TWIST PP