The following data is part of a premarket notification filed by Haemonetics Corporation with the FDA for Processing Systems For Frozen Blood.
Device ID | BK840025 |
510k Number | BK840025 |
Device Name: | Processing Systems For Frozen Blood |
Classification | System, Processing For Frozen Blood |
Applicant | Haemonetics Corporation 400 Wood Road Braintree, MA 02184 |
Product Code | KSW |
CFR Regulation Number | 864.9145 [🔎] |
Decision | Substantially Equivalent (SE) |
Type | 510(k) Traditio |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1984-09-25 |
Decision Date | 1984-11-14 |