FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

RESOUND PORTABLE PRESCRIPTIVE PROGRAMMING SYSTEM

K Number: K931372 · Decision Nov 3, 1993
Classifications
1
FEI Numbers
101
Registration Numbers
101
Same Product Code
1366
Applicant Total
41
Review Days
231

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Basic Information

Device Name
RESOUND PORTABLE PRESCRIPTIVE PROGRAMMING SYSTEM
K Number
K931372
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
874.3300
Medical Specialty
Ear, Nose, Throat
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Resound Corp.
Date Received
March 17, 1993
Decision Date
November 3, 1993
Product Code
ESD
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
ESD Hearing Aid, Air-Conduction, Prescription

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Other Clearances by Resound Corp.

K Number Device Name
K984547 DIGITAL LGOB PROCEDURE USING RESOUND, DIGITAL 5000 SERIES HEARING AIDS
K974081 RESOUND STEALTH CIC
K974257 RESOUND DIGITAL 2000-BT W/DIGITAL 2000-DF (DIGITAL PROGRAMMER)
K971605 RESOUND ED4 PERSONAL HEARING SYSTEM W/REMOTE CONTROL OPTION
K970215 AUDALLION II HEARING SYSTEM
K964557 RESOUND BT4 PERSONAL HEARING SYSTEM W/REMOTE CONTROL OPTION
K964115 RESOUND CC4 PERSONAL HEARING SYSTEM
K960684 HEARING AID - AIR CONDUCTION
K960680 RESOUND PERSONAL HEARING SYSTEMS EDR ENCORE SERIES MODELS EDR-E, EDR-ES, EDR-EV, & EDR-P1
K960052 RESOUND PERSONAL HEARING SYSTEM BT2-ES, BT2-EV, & BT241
Search all 41 clearances from Resound Corp. →