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

PERSONAL HEARING SYSTEM

K Number: K944041 · Decision Dec 27, 1994
Classifications
1
FEI Numbers
68
Registration Numbers
68
Same Product Code
29
Applicant Total
41
Review Days
131

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Basic Information

Device Name
PERSONAL HEARING SYSTEM
K Number
K944041
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5200
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Resound Corp.
Date Received
August 18, 1994
Decision Date
December 27, 1994
Product Code
LRS
Advisory Committee
General Hospital
Review Advisory Committee
SU
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
LRS I.V. Start Kit

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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. →