The following data is part of a premarket notification filed by Rion Acoustic Instruments, Inc. with the FDA for Rionet Hearing Aid And/or Rion #hb-70.
Device ID | K801692 |
510k Number | K801692 |
Device Name: | RIONET HEARING AID AND/OR RION #HB-70 |
Classification | Hearing Aid, Air Conduction |
Applicant | RION ACOUSTIC INSTRUMENTS, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
Product Code | ESD |
CFR Regulation Number | 874.3300 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1980-07-23 |
Decision Date | 1980-08-14 |