Teknar, Inc.
Mchenry, IL, US
Teknar, Inc. appears in FDA device records in Mchenry, IL. FDA records list 18 510(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
- 18
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 18 510(k) clearances for Teknar, Inc. between 1980 and 1990. The busiest year on record is 1988, with 4. The most recent is 1990, with 3.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1980 | 1 |
| 1981 | 1 |
| 1982 | 2 |
| 1983 | 1 |
| 1984 | 1 |
| 1985 | 1 |
| 1986 | 1 |
| 1987 | 2 |
| 1988 | 4 |
| 1989 | 1 |
| 1990 | 3 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K903666 | OPHTHASONIC A/P III | HPY | Substantially Equivalent | |
| K896038 | B-SCAN 10 MHZ PROBE | ITX | Substantially Equivalent | |
| K896150 | IMAGE 2000 SYSTEM, IMAGING, ULTRA-SONIC | IYO | Substantially Equivalent | |
| K891777 | PRO-CUT BIOPSY NEEDLE | FCG | Substantially Equivalent | |
| K883965 | PROBE, IMAGING, ULTRASONIC, MECHANICAL SECTOR | IYO | Substantially Equivalent | |
| K881850 | TEKNAR PERCU-SCAN | IYO | Substantially Equivalent | |
| K881605 | BIOPSY GUIDE | IYO | Substantially Equivalent | |
| K880659 | TEKNAR PROSCAN ACCESSORY PROBE | IYO | Substantially Equivalent | |
| K871536 | OPHTHASONIC A-SCAN/ B-SCAN | IYO | Substantially Equivalent for Some Indications | |
| K864807 | TEKNAR PROSCAN(TM) | IYO | Substantially Equivalent | |
| K860757 | OPHTHASONIC A-SCAN | IYO | Substantially Equivalent | |
| K850116 | BETASONIC III | IYO | Substantially Equivalent | |
| K834539 | AXIPAC II | Substantially Equivalent | ||
| K830474 | IV STAND | HQC | Substantially Equivalent | |
| K823011 | VC III | EPT | Substantially Equivalent | |
| K822900 | FISCH DRILL PUMP | Substantially Equivalent | ||
| K810697 | AXISONIC II | HDR | Substantially Equivalent | |
| K801314 | VOCON MODEL VC526 | FSO | 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