The following data is part of a premarket notification filed by Haemonetics Corporation with the FDA for Empty Containers For The Collection & Processing Of Blood/blood Components.
Device ID | BK020001 |
510k Number | BK020001 |
Device Name: | Empty Containers For The Collection & Processing Of Blood/Blood Components |
Classification | Container, Empty, For Collection & Processing Of Blood & Blood Components |
Applicant | Haemonetics Corporation 400 Wood Road Braintree, MA 02184 |
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 | 2002-01-22 |
Decision Date | 2002-03-29 |
Device Identifier | submissionNumber | Supplement |
---|---|---|
30812747011673 | BK020001 | 0 |
30812747011536 | BK020001 | 0 |
30812747011529 | BK020001 | 0 |
30812747019228 | BK020001 | 0 |
00812747019807 | BK020001 | 0 |