The following data is part of a premarket notification filed by E-z-em, Inc. with the FDA for Endodynamics Siegel Theraputic Stent.
| Device ID | K853666 |
| 510k Number | K853666 |
| Device Name: | ENDODYNAMICS SIEGEL THERAPUTIC STENT |
| Classification | Stents, Drains And Dilators For The Biliary Ducts |
| Applicant | E-Z-EM, INC. 717 MAIN ST. Westbury, NY 11590 |
| Contact | Jack T Berger |
| Correspondent | Jack T Berger E-Z-EM, INC. 717 MAIN ST. Westbury, NY 11590 |
| Product Code | FGE |
| CFR Regulation Number | 876.5010 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1985-09-03 |
| Decision Date | 1985-11-05 |