The following data is part of a premarket notification filed by Strato Medical Corp. with the FDA for Lifeport Ii, Model Lps-1100.
| Device ID | K881075 |
| 510k Number | K881075 |
| Device Name: | LIFEPORT II, MODEL LPS-1100 |
| 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 | 1988-03-14 |
| Decision Date | 1988-06-03 |