The following data is part of a premarket notification filed by Strato Medical Corp. with the FDA for Lifeport Polyurethane Catheter.
| Device ID | K895871 |
| 510k Number | K895871 |
| Device Name: | LIFEPORT POLYURETHANE CATHETER |
| Classification | Port & Catheter, Implanted, Subcutaneous, Intravascular |
| Applicant | STRATO MEDICAL CORP. 123 BRIMBAL AVE. P.O.B.3148 Beverly, MA 01915 |
| Contact | Joseph Ress |
| Correspondent | Joseph Ress STRATO MEDICAL CORP. 123 BRIMBAL AVE. P.O.B.3148 Beverly, MA 01915 |
| Product Code | LJT |
| CFR Regulation Number | 880.5965 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1989-10-04 |
| Decision Date | 1989-11-17 |