The following data is part of a premarket notification filed by Heartport, Inc. with the FDA for Heartport Endoaortic Clamp.
| Device ID | K955132 |
| 510k Number | K955132 |
| Device Name: | HEARTPORT ENDOAORTIC CLAMP |
| Classification | Clamp, Vascular |
| Applicant | HEARTPORT, INC. 200 CHESAPEAKE DR. Redwood City, CA 94063 |
| Contact | David A Tucker |
| Correspondent | David A Tucker HEARTPORT, INC. 200 CHESAPEAKE DR. Redwood City, CA 94063 |
| Product Code | DXC |
| CFR Regulation Number | 870.4450 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1995-11-09 |
| Decision Date | 1996-06-07 |
| Summary: | summary |