The following data is part of a premarket notification filed by Atrium Medical Corp. with the FDA for Atrium's Hybrid Ptfe.
| Device ID | K933391 |
| 510k Number | K933391 |
| Device Name: | ATRIUM'S HYBRID PTFE |
| Classification | Prosthesis, Vascular Graft, Of Less Then 6mm Diameter |
| Applicant | ATRIUM MEDICAL CORP. 17 CLINTON DR. Hollis, NH 03049 |
| Contact | Ted Karwoski |
| Correspondent | Ted Karwoski ATRIUM MEDICAL CORP. 17 CLINTON DR. Hollis, NH 03049 |
| Product Code | DYF |
| CFR Regulation Number | 870.3450 [🔎] |
| Decision | Se - Postmarket Surveillance Required (SESP) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1993-07-12 |
| Decision Date | 1994-12-15 |