The following data is part of a premarket notification filed by Electone, Inc. with the FDA for Silver Ultra Mini Canal.
Device ID | K950458 |
510k Number | K950458 |
Device Name: | SILVER ULTRA MINI CANAL |
Classification | Hearing Aid, Air Conduction |
Applicant | ELECTONE, INC. 1124 FLORIDA CENTRAL PKWY. Longwood, FL 32750 |
Contact | Jim Nee |
Correspondent | Jim Nee ELECTONE, INC. 1124 FLORIDA CENTRAL PKWY. Longwood, FL 32750 |
Product Code | ESD |
CFR Regulation Number | 874.3300 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1995-02-03 |
Decision Date | 1995-03-31 |