The following data is part of a premarket notification filed by Pall Biomedical Products Co. with the FDA for Ultipor Blood Filter Extra-corporeal.
| Device ID | K791748 |
| 510k Number | K791748 |
| Device Name: | ULTIPOR BLOOD FILTER EXTRA-CORPOREAL |
| Classification | Filter, Blood, Cardiopulmonary Bypass, Arterial Line |
| Applicant | PALL BIOMEDICAL PRODUCTS CO. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | DTM |
| CFR Regulation Number | 870.4260 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1979-09-10 |
| Decision Date | 1979-10-02 |