The following data is part of a premarket notification filed by Terumo Bct, Inc with the FDA for Automated Blood Cell Separator -filtration.
Device ID | BK020041 |
510k Number | BK020041 |
Device Name: | Automated Blood Cell Separator -Filtration |
Classification | Separator, Automated, Blood Cell, Diagnostic |
Applicant | Terumo BCT, Inc 10811 W. Collins Ave. Lakewood, CO 80215 US |
Product Code | GKT |
CFR Regulation Number | 864.9245 [🔎] |
Decision | Substantially Equivalent (SE) |
Type | 510(k) Traditio |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2002-09-18 |
Decision Date | 2003-04-23 |
Device Identifier | submissionNumber | Supplement |
---|---|---|
35020583706294 | BK020041 | 0 |
35020583706201 | BK020041 | 0 |
05020583706200 | BK020041 | 0 |
05020583706293 | BK020041 | 0 |