The following data is part of a premarket notification filed by Starkey Laboratories, Inc. with the FDA for Starket Model Hms.
Device ID | K844275 |
510k Number | K844275 |
Device Name: | STARKET MODEL HMS |
Classification | Calibrator, Hearing Aid / Earphone And Analysis Systems |
Applicant | STARKEY LABORATORIES, INC. 6700 WASHINGTON AVE. SOUTH Eden Prairie, MN 55344 |
Contact | Jim Gilbertsen |
Correspondent | Jim Gilbertsen STARKEY LABORATORIES, INC. 6700 WASHINGTON AVE. SOUTH Eden Prairie, MN 55344 |
Product Code | ETW |
CFR Regulation Number | 874.3310 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1984-11-05 |
Decision Date | 1984-12-03 |