The following data is part of a premarket notification filed by Cascade Medical Enterprises, Llc with the FDA for Blood Bank Supplies.
| Device ID | BK020051 |
| 510k Number | BK020051 |
| Device Name: | Blood Bank Supplies |
| Classification | Supplies, Blood-bank |
| Applicant | Cascade Medical Enterprises, LLC 20 Greenup Court Wayne, NJ 07470 US |
| Product Code | KSS |
| CFR Regulation Number | 864.9050 [🔎] |
| Decision | Substantially Equivalent (SE) |
| Type | 510(k) Traditio |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2002-11-04 |
| Decision Date | 2002-12-20 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 00859070006043 | BK020051 | 0 |
| 00859070006036 | BK020051 | 0 |
| 00859070006029 | BK020051 | 0 |
| 00859070006012 | BK020051 | 0 |
| 00859070006005 | BK020051 | 0 |