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

TRACOR RA 410 AUDIOMETER

K Number: K780450 · Decision Mar 30, 1978
Classifications
1
FEI Numbers
62
Registration Numbers
62
Same Product Code
234
Applicant Total
10
Review Days
10

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Basic Information

Device Name
TRACOR RA 410 AUDIOMETER
K Number
K780450
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
874.1050
Medical Specialty
Ear, Nose, Throat
Decision
Substantially Equivalent
Applicant
Tracor Instruments, Inc.
Date Received
March 20, 1978
Decision Date
March 30, 1978
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 Tracor Instruments, Inc.

K Number Device Name
K853245 TRACOR MODEL RA600 MICROPROCESSOR AUDIOMETER
K851392 TRACOR 200 MICROPROCESSOR AUDIOMETER/TRACOR RA 200
K822414 TRACOR RA400 AUDIOMETER
K790903 TRACOR MODEL RA-411 MICROPROCESSOR
K781704 STIMULATOR, TN-3001 SOMATOSENSORY
K781743 RESPONSE SYSTEM, TN-3000
K780749 SPEECH AUDIOMETER RA 226
K780474 AUDIOMETER CALIBRATOR MODEL RA 310
K760859 TRACOR MODEL RA 208 COMPLIANCE AUDIOM