Stereo Optical Company LLC
Chicago, IL, US
STEREO OPTICAL COMPANY LLC appears in FDA device records in Chicago, IL. FDA records list 5 510(k) clearances between and , no PMA records and one registered establishment. As of , FDA records show no recalls for this company, and at least one establishment registration is current.
FDA records held for this company
510(k) clearance history
FDA records hold 5 510(k) clearances for Stereo Optical Company LLC between 1984 and 1993. The busiest year on record is 1984, with 1. The most recent is 1993, with 1.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1984 | 1 |
| 1986 | 1 |
| 1988 | 1 |
| 1991 | 1 |
| 1993 | 1 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K924741 | OPTEC 3000 | HKO | Substantially Equivalent | |
| K904828 | OPTEC 2300 AFVT, ARMED FORCES VISION TESTER | HKO | Substantially Equivalent | |
| K875237 | OPTEC 1000 DMV VISION TESTER MODIFY | HOX | Substantially Equivalent | |
| K863509 | OPTEC 1000 DMV | HOX | Substantially Equivalent | |
| K843042 | VISION TESTER | HKO | Substantially Equivalent |
Registered establishments
| Registration | FEI | Establishment | Address | Registration expires | Product codes listed |
|---|---|---|---|---|---|
| 1419226 | 1419226 | STEREO OPTICAL COMPANY LLC | 8600 W Catalpa Ave Ste 703, CHICAGO, IL 60656 US | 2026 |
Registration numbers link to the FDA registration and listing record for that establishment.
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