The following data is part of a premarket notification filed by Scanlan Intl., Inc. with the FDA for Scanlan Endarsector.
| Device ID | K841521 |
| 510k Number | K841521 |
| Device Name: | SCANLAN ENDARSECTOR |
| Classification | Stripper, Artery, Intraluminal |
| Applicant | SCANLAN INTL., INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | DWX |
| CFR Regulation Number | 870.4875 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1984-04-12 |
| Decision Date | 1984-08-03 |