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

DANPLEX SCREENING AUDIOMETER

K Number: K923074 · Decision Sep 23, 1992
Classifications
1
FEI Numbers
62
Registration Numbers
62
Same Product Code
234
Applicant Total
68
Review Days
90

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Basic Information

Device Name
DANPLEX SCREENING AUDIOMETER
K Number
K923074
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
Life-Tech Intl., Inc.
Date Received
June 25, 1992
Decision Date
September 23, 1992
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

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Other Clearances by Life-Tech Intl., Inc.

K Number Device Name
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K954505 EZ STIM
K954315 PVC ABDOMINAL/RECTAL PRESSURE CATHETER
K954341 URODYNAMICS TUBING AND INFUSION SETS
K953451 UROPUMP TUBE & DAMPING CHAMGER
K953353 UROVISION JANUS
K946108 EAR-A-GATOR
K913601 MICROPHOR
K940203 TRIPLE LUMEN URODYNAMIC CATHETER WITH RADIOPAQUE MARKERS
Search all 68 clearances from Life-Tech Intl., Inc. →