The following data is part of a premarket notification filed by The Binding Site Group, Ltd. with the FDA for Human Iga Csf Kit For Use On Spaplus.
Device ID | K120901 |
510k Number | K120901 |
Device Name: | HUMAN IGA CSF KIT FOR USE ON SPAPLUS |
Classification | Method, Nephelometric, Immunoglobulins (g, A, M) |
Applicant | THE BINDING SITE GROUP, LTD. 8 CALTHORPE ROAD Edgbaston, GB B15 1qt |
Contact | Jill Constantine |
Correspondent | Jill Constantine THE BINDING SITE GROUP, LTD. 8 CALTHORPE ROAD Edgbaston, 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 | 2012-03-26 |
Decision Date | 2013-05-30 |
Device Identifier | submissionNumber | Supplement |
---|---|---|
05051700016162 | K120901 | 000 |