Scimage, Inc.
Los Altos, CA, US
SCIMAGE, INC. appears in FDA device records in Los Altos, CA. FDA records list 3 510(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 3 510(k) clearances for Scimage, Inc. between 1996 and 2008. The busiest year on record is 1996, with 1. The most recent is 2008, with 1.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1996 | 1 |
| 2001 | 1 |
| 2008 | 1 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K073169 | SCIMAGE PICOMENTERPRISE | LLZ | Substantially Equivalent | |
| K003484 | NETRA WORKSTATION AND NETRAMD SOFTWARE | LLZ | Substantially Equivalent | |
| K960911 | NETRA WORKSTATION SYSTEM & NETRA MD SOFTWARE | LMD | Substantially Equivalent |
Registered establishments
| Registration | FEI | Establishment | Address | Registration expires | Product codes listed |
|---|---|---|---|---|---|
| 2952596 | 3000206530 | SCIMAGE, INC. | 4916 EL CAMINO REAL, SUITE 200, LOS ALTOS, CA 94022 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