The following data is part of a premarket notification filed by Light Diagnostics with the FDA for Poliovirus 1 Monoclonal Antibody.
Device ID | K940018 |
510k Number | K940018 |
Device Name: | POLIOVIRUS 1 MONOCLONAL ANTIBODY |
Classification | Antisera, Fluorescent, Poliovirus 1-3 |
Applicant | LIGHT DIAGNOSTICS 28835 SINGLE OAK DR. Temecula, CA 92590 |
Contact | Richard P Triglia |
Correspondent | Richard 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 | 1994-01-04 |
Decision Date | 1995-09-08 |
Device Identifier | submissionNumber | Supplement |
---|---|---|
04053252369407 | K940018 | 000 |