The following data is part of a premarket notification filed by The Binding Site Group Ltd with the FDA for Optilite Igg4 Kit.
Device ID | K150526 |
510k Number | K150526 |
Device Name: | Optilite IgG4 Kit |
Classification | Method, Nephelometric, Immunoglobulins (g, A, M) |
Applicant | THE BINDING SITE GROUP LTD 8 CALTHORPE ROAD EDGBASTON Birmingham, West Midlands, GB B15 1qt |
Contact | Andrea Thomas |
Correspondent | Andrea Thomas THE BINDING SITE GROUP LTD 8 CALTHORPE ROAD EDGBASTON Birmingham, West Midlands, GB B15 1qt |
Product Code | CFN |
CFR Regulation Number | 866.5510 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2015-03-02 |
Decision Date | 2015-05-30 |
Device Identifier | submissionNumber | Supplement |
---|---|---|
05051700017558 | K150526 | 000 |