The following data is part of a premarket notification filed by Light Diagnostics with the FDA for Poliovirus Blend Monoclonal Antibodies.
| Device ID | K940026 |
| 510k Number | K940026 |
| Device Name: | POLIOVIRUS BLEND MONOCLONAL ANTIBODIES |
| Classification | Antisera, Fluorescent, Poliovirus 1-3 |
| Applicant | LIGHT DIAGNOSTICS 28835 SINGLE OAK DR. Temecula, CA 92590 |
| Contact | Rihcard P Triglia |
| Correspondent | Rihcard P Triglia LIGHT DIAGNOSTICS 28835 SINGLE OAK DR. Temecula, CA 92590 |
| Product Code | GOE |
| CFR Regulation Number | 866.3405 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1994-01-03 |
| Decision Date | 1995-09-12 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 04053252338243 | K940026 | 000 |