The following data is part of a premarket notification filed by Xomed, Inc. with the FDA for Additional Indications For Xomed Audiant Bone Con..
Device ID | K875277 |
510k Number | K875277 |
Device Name: | ADDITIONAL INDICATIONS FOR XOMED AUDIANT BONE CON. |
Classification | Hearing Aid, Bone Conduction |
Applicant | XOMED, INC. 6743 SOUTHPOINT DR. NORTH Jacksonville, FL 32216 -0980 |
Contact | Donald R Bruce |
Correspondent | Donald R Bruce XOMED, INC. 6743 SOUTHPOINT DR. NORTH Jacksonville, FL 32216 -0980 |
Product Code | LXB |
CFR Regulation Number | 874.3300 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1987-12-24 |
Decision Date | 1988-03-14 |