Telesonic, Inc.
Mchenry, IL, US
Telesonic, Inc. appears in FDA device records in Mchenry, IL. FDA records list 12 510(k) clearances between and , no PMA records and no registered establishments. As of , FDA records show no recalls for this company.
FDA records held for this company
- 510(k) clearances
- 12
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 12 510(k) clearances for Telesonic, Inc. between 1980 and 1987. The busiest year on record is 1980, with 6. The most recent is 1987, with 1.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1980 | 6 |
| 1981 | 3 |
| 1982 | 2 |
| 1987 | 1 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K872606 | TELESONIC BODY STIMULATOR | IPF | Substantially Equivalent | |
| K813330 | POST-AURICULAR HEARING AID MODEL S-101 | ESD | Substantially Equivalent | |
| K813329 | POST-AURICULAR HEARING AID MODEL P-101 | ESD | Substantially Equivalent | |
| K813344 | POST-AURICULAR HEARING AID MODEL ASP-103 | ESD | Substantially Equivalent | |
| K813316 | CUSTOM-IN-THE-EAR HEARING AID | ESD | Substantially Equivalent | |
| K811031 | TELESONIC & ARCON | ESD | Substantially Equivalent | |
| K802597 | TELESONIC ARCON & SOUNDEX ASP 101 | ESD | Substantially Equivalent | |
| K802596 | TELESONIC, ARCON & SOUNDEX ASP 102 | ESD | Substantially Equivalent | |
| K801067 | TELESONIC, GENERIC & SOUNDEX C-102 | ESD | Substantially Equivalent | |
| K801066 | TELESONIC, SOUNDEX & GENERIC V-101 | ESD | Substantially Equivalent | |
| K800105 | TELESONIC (HEARING AID) | ESD | Substantially Equivalent | |
| K792644 | TELESONIC V-101 | ESD | Substantially Equivalent |
Registered establishments
No FDA establishment registrations recorded against this company.
FDA product codes
Recall records
No recall records for this company in the ingested FDA data.
Verification record
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Data as of , FDA export datePage updated Source: openFDA, public domain