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

RASTRONICS CCI 10/3 HEARING AID ANALYSIS

K Number: K902252 · Decision Sep 12, 1990
Classifications
1
FEI Numbers
15
Registration Numbers
15
Same Product Code
45
Applicant Total
5
Review Days
114

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Basic Information

Device Name
RASTRONICS CCI 10/3 HEARING AID ANALYSIS
K Number
K902252
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
874.3310
Medical Specialty
Ear, Nose, Throat
Decision
Substantially Equivalent
Applicant
Rastronics USA, Inc.
Date Received
May 21, 1990
Decision Date
September 12, 1990
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 Rastronics USA, Inc.

K Number Device Name
K902244 RASTRONICS CCI 8
K902287 RASTRONICS PORTAREM 20
K890864 HANDTYMP SCREENER MODEL 2000 + 2002 REMOTE TRANS.
K853320 FREQUENCY RESPONSE ANALYZER COMPUTER SYS CCI-10