The following data is part of a premarket notification filed by Haemonetics Manufacturing Inc. with the FDA for Empty Containers For The Collection & Processing Of Blood/blood Components.
Device ID | BK160027 |
510k Number | BK160027 |
Device Name: | Empty Containers For The Collection & Processing Of Blood/Blood Components |
Classification | Container, Empty, For Collection & Processing Of Blood & Blood Components |
Applicant | Haemonetics Manufacturing Inc. 1630 Industrial Park Street Covina, CA 91722 |
Product Code | KSR |
CFR Regulation Number | 864.9100 [🔎] |
Decision | Substantially Equivalent (SE) |
Type | 510(k) Special |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2016-03-18 |
Decision Date | 2016-05-16 |