The following data is part of a premarket notification filed by Extracorporeal Medical Specialities, Inc. with the FDA for Intersept 40 Micron Filter.
| Device ID | K833477 |
| 510k Number | K833477 |
| Device Name: | INTERSEPT 40 MICRON FILTER |
| Classification | Filter, Blood, Cardiopulmonary Bypass, Arterial Line |
| Applicant | EXTRACORPOREAL MEDICAL SPECIALITIES, INC. 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 | 1983-10-07 |
| Decision Date | 1983-12-27 |