The following data is part of a premarket notification filed by Oxford Laboratories, Inc. with the FDA for Serum, Alpha-1-glycoprotein Anti-human.
Device ID | K760143 |
510k Number | K760143 |
Device Name: | SERUM, ALPHA-1-GLYCOPROTEIN ANTI-HUMAN |
Classification | Alpha-1-b-glycoprotein, Antigen, Antiserum, Control |
Applicant | OXFORD LABORATORIES, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
Product Code | DEX |
CFR Regulation Number | 866.5420 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1976-06-29 |
Decision Date | 1976-07-20 |