The following data is part of a premarket notification filed by Unitron Industries, Inc. with the FDA for Unitron Model Sound F/xd +4 (sound F/xd +4).
Device ID | K964511 |
510k Number | K964511 |
Device Name: | UNITRON MODEL SOUND F/XD +4 (SOUND F/XD +4) |
Classification | Hearing Aid, Air Conduction |
Applicant | UNITRON INDUSTRIES, INC. 3555 WALNUT ST. P.O. BOX 5010 Port Huron, MI 48061 -5010 |
Contact | Jerry G Johnson |
Correspondent | Jerry G Johnson UNITRON INDUSTRIES, INC. 3555 WALNUT ST. P.O. BOX 5010 Port Huron, MI 48061 -5010 |
Product Code | ESD |
CFR Regulation Number | 874.3300 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1996-11-08 |
Decision Date | 1996-11-27 |
Summary: | summary |