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

INTERACOUSTICS HEARING AID ANALYZER MS 40

K Number: K943607 · Decision Sep 23, 1994
Classifications
1
FEI Numbers
15
Registration Numbers
15
Same Product Code
45
Applicant Total
9
Review Days
60

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Basic Information

Device Name
INTERACOUSTICS HEARING AID ANALYZER MS 40
K Number
K943607
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
874.3310
Medical Specialty
Ear, Nose, Throat
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Precision Acoustics Ind., Inc.
Date Received
July 25, 1994
Decision Date
September 23, 1994
Product Code
ETW
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
ETW Calibrator, Hearing Aid / Earphone And Analysis Systems

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (ETW), ordered by most recent decision date.

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Other Clearances by Precision Acoustics Ind., Inc.

K Number Device Name
K941920 INTERACOUSTICS CLINICAL AUDIOMETER
K943066 INTERACOUSTICS COMPUTER AUDIOMETER BA 20
K942008 INTERACOUSTICS AUTOMATIC IMPEDANCE AUDIOMETER
K942007 INTERACOUSTICS CLINICAL IMPEDANCE AUDIOMETER AZ26
K943065 INTERACOUSTICS CLINICAL AUDIOMETER
K942006 INTERACOUSTICS DIAGNOSTIC AUDIOMETER
K941848 INTERACOUSTICS. HEARING AID ANALYZER
K930260 ACOUSTIC ANALYZER AA30