510(k) K923071

DANPLEX DIAGNOSTIC AUDIOMETER, CLIN. DIAG. AUDIOMT by Life-Tech Intl., Inc. — Product Code ESD

K923071 is an FDA 510(k) premarket notification submitted by Life-Tech Intl., Inc. for the device "DANPLEX DIAGNOSTIC AUDIOMETER, CLIN. DIAG. AUDIOMT". The FDA issued a decision of Substantially Equivalent on September 28, 1992. The device falls under product code ESD (Hearing Aid, Air-Conduction, Prescription), a Class I device regulated under 21 CFR 874.3300. Life-Tech Intl., Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
September 28, 1992
Date Received
June 25, 1992
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Hearing Aid, Air-Conduction, Prescription
Device Class
Class I
Regulation Number
874.3300
Review Panel
EN
Submission Type

An air-conduction hearing aid is a wearable sound amplifying device intended to compensate for impaired hearing that conducts sound to the ear through the air. This is a prescription hearing aid.