The following data is part of a premarket notification filed by Lin-zhi International, Inc. with the FDA for Oxycodone Enzyme Immunoassay And Oxycodone Calibrators And Controls.
Device ID | K050733 |
510k Number | K050733 |
Device Name: | OXYCODONE ENZYME IMMUNOASSAY AND OXYCODONE CALIBRATORS AND CONTROLS |
Classification | Enzyme Immunoassay, Opiates |
Applicant | Lin-Zhi International, Inc. 687 NORTH PASTORIA AVE. Sunnyvale, CA 94085 -2917 |
Contact | Cheng-i Lin |
Correspondent | Cheng-i Lin Lin-Zhi International, Inc. 687 NORTH PASTORIA AVE. Sunnyvale, CA 94085 -2917 |
Product Code | DJG |
Subsequent Product Code | DLJ |
Subsequent Product Code | LAS |
CFR Regulation Number | 862.3650 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2005-03-17 |
Decision Date | 2005-06-13 |
Summary: | summary |