Syntex Corp.
Mchenry, IL, US
Syntex Corp. appears in FDA device records in Mchenry, IL. FDA records list 10 510(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
- 10
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 10 510(k) clearances for Syntex Corp. between 1976 and 1992. The busiest year on record is 1976, with 4. The most recent is 1992, with 1.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1976 | 4 |
| 1977 | 1 |
| 1978 | 3 |
| 1984 | 1 |
| 1992 | 1 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K920314 | TXIT D.A.U. BARBITURATE ASSAY (MODIFICATION) | DIS | Substantially Equivalent | |
| K843593 | SURGIPRESS SURGICAL LOOP | HRQ | Substantially Equivalent | |
| K780997 | AMALGAM ALLOY | EJJ | Substantially Equivalent | |
| K780769 | S-100 CT SCANNER | JAK | Substantially Equivalent | |
| K780483 | FIBER OPTIC HANDPIECE | EFB | Substantially Equivalent | |
| K761331 | OPUS I OPTION - FIBER OPTIC L SYSTEM | EAY | Substantially Equivalent | |
| K761332 | HI-SENSITIVITY MODE OPTION FOR S60-1A | JAK | Substantially Equivalent | |
| K761330 | SYNTEX SYSTEM 6000 | JAK | Substantially Equivalent | |
| K761264 | OPTIONS FOR STAR DENTAL OPUS I | DYN | Substantially Equivalent | |
| K761033 | COMPUTERIZED TOMOGRAPHY SCANNER | JAK | 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