The following data is part of a premarket notification filed by Starkey Laboratories, Inc. with the FDA for Pro-connect.
| Device ID | K932269 | 
| 510k Number | K932269 | 
| Device Name: | PRO-CONNECT | 
| Classification | Hearing Aid, Air Conduction | 
| Applicant | STARKEY LABORATORIES, INC. 6700 WASHINGTON AVE. SOUTH Eden Prairie, MN 55344 | 
| Contact | Jerrold Lang | 
| Correspondent | Jerrold Lang STARKEY LABORATORIES, INC. 6700 WASHINGTON AVE. SOUTH Eden Prairie, MN 55344 | 
| Product Code | ESD | 
| CFR Regulation Number | 874.3300 [🔎] | 
| Decision | Substantially Equivalent (SESE) | 
| Type | Traditional | 
| 3rd Party Reviewed | No | 
| Combination Product | No | 
| Date Received | 1993-05-11 | 
| Decision Date | 1994-05-13 | 
| Mark Image Registration | Serial | Company Trademark Application Date | 
|---|---|
|  PRO-CONNECT  85148219  not registered Dead/Abandoned | Topps Products, Inc. 2010-10-08 |