The following data is part of a premarket notification filed by Unipath Ltd. with the FDA for Immunoglobulins A.
Device ID | K873869 |
510k Number | K873869 |
Device Name: | IMMUNOGLOBULINS A |
Classification | Iga, Antigen, Antiserum, Control |
Applicant | UNIPATH LTD. NORSE ROAD Bedford Mk41 Oqg, GB |
Contact | George Zajicek |
Correspondent | George Zajicek UNIPATH LTD. NORSE ROAD Bedford Mk41 Oqg, GB |
Product Code | CZP |
CFR Regulation Number | 866.5510 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1987-08-24 |
Decision Date | 1987-10-13 |