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

REXTON RX12 POWER PLUS W/DUAL RECEIVER

K Number: K901341 · Decision Jul 27, 1990
Classifications
1
FEI Numbers
117
Registration Numbers
117
Same Product Code
1366
Applicant Total
21
Review Days
127

Basic Information

Device Name
REXTON RX12 POWER PLUS W/DUAL RECEIVER
K Number
K901341
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
874.3300
Medical Specialty
Ear, Nose, Throat
Decision
Substantially Equivalent
Applicant
REXTON, INC.
Date Received
March 22, 1990
Decision Date
July 27, 1990
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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K960295 LONG LIFE RX-12
K954922 REXTON'S HORIZION FAMILY OF MULTIPLE SITUATION, SINGLE CHANNEL PROGRAMMBALE INSTRUMENTS
K953770 REXTON MINI-PRIMO PLUS, PP142, D.C .H.I. FAMILY
K950451 M-29 PP-PC, M-29 PP-O/PC
K944851 MICRO MINI PRIMO AGC, MICRO-MINI PRIMO S-AGC
K944777 ORION PPM, PP, PP-D
K944359 EXPRESSION RX-12, ENHANCEMENT RX-34, ELITE RX-12
K942702 DEEP CANAL HEARING INSTRUMENT
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