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

HEARING AID HB-72 RIONET

K Number: K823384 · Decision Dec 9, 1982
Classifications
1
FEI Numbers
101
Registration Numbers
101
Same Product Code
1366
Applicant Total
4
Review Days
27

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
HEARING AID HB-72 RIONET
K Number
K823384
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
874.3300
Medical Specialty
Ear, Nose, Throat
Decision
Substantially Equivalent
Applicant
Kindel & Anderson
Date Received
November 12, 1982
Decision Date
December 9, 1982
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

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (ESD), ordered by most recent decision date.

View all

Other Clearances by Kindel & Anderson

K Number Device Name
K823383 HEARING AID HB-33 RIONET
K802870 RION ELECTRO-PALATOGRAPH MODEL DP-01
K802812 RIONET HEARING AID