The following data is part of a premarket notification filed by Light Diagnostics with the FDA for Poliovirus 2 Monoclonal Antibody.
Device ID | K940034 |
510k Number | K940034 |
Device Name: | POLIOVIRUS 2 MONOCLONAL ANTIBODY |
Classification | Antisera, Fluorescent, Poliovirus 1-3 |
Applicant | LIGHT DIAGNOSTICS 27520 ENTERPRISE CIRCLE WEST Temecula, CA 92390 |
Contact | Richard P Triglia |
Correspondent | Richard P Triglia LIGHT DIAGNOSTICS 27520 ENTERPRISE CIRCLE WEST Temecula, CA 92390 |
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 | 1995-09-12 |
Device Identifier | submissionNumber | Supplement |
---|---|---|
04053252677649 | K940034 | 000 |