The following data is part of a premarket notification filed by Bio-rad Laboratories, Inc. with the FDA for Access Vitamin B12 Assay (modification).
Device ID | K955436 |
510k Number | K955436 |
Device Name: | ACCESS VITAMIN B12 ASSAY (MODIFICATION) |
Classification | Radioassay, Vitamin B12 |
Applicant | BIO-RAD LABORATORIES, INC. 1000 LAKE HAZELTINE DR. Chaska, MN 55318 -1084 |
Contact | Dennis Griffin |
Correspondent | Dennis Griffin BIO-RAD LABORATORIES, INC. 1000 LAKE HAZELTINE DR. Chaska, MN 55318 -1084 |
Product Code | CDD |
CFR Regulation Number | 862.1810 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1995-10-02 |
Decision Date | 1996-01-24 |