Submission Details
| 510(k) Number | K941133 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | March 09, 1994 |
| Decision Date | May 12, 1994 |
| Days to Decision | 64 days |
| Submission Type | Traditional |
| Review Panel | Ear, Nose, Throat (EN) |
| Summary | Summary PDF |
K941133 is an FDA 510(k) clearance for the 770-ATC, a Hearing Aid, Air-conduction, Prescription (Class I — General Controls, product code ESD), submitted by Electone, Inc. (Longwood, US). The FDA issued a Cleared decision on May 12, 1994, 64 days after receiving the submission on March 9, 1994. This device falls under the Ear, Nose, Throat review panel. Regulated under 21 CFR 874.3300.
| 510(k) Number | K941133 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | March 09, 1994 |
| Decision Date | May 12, 1994 |
| Days to Decision | 64 days |
| Submission Type | Traditional |
| Review Panel | Ear, Nose, Throat (EN) |
| Summary | Summary PDF |
| Product Code | ESD — Hearing Aid, Air-conduction, Prescription |
| Device Class | Class I — General Controls |
| CFR Regulation | 21 CFR 874.3300 |
| Definition | An Air-conduction Hearing Aid Is A Wearable Sound Amplifying Device Intended To Compensate For Impaired Hearing That Conducts Sound To The Ear Through The Air. This Is A Prescription Hearing Aid. |