The following data is part of a premarket notification filed by Strato Medical Corp. with the FDA for Lifeport Low Profile Vascular Access Port W/cath..
Device ID | K880305 |
510k Number | K880305 |
Device Name: | LIFEPORT LOW PROFILE VASCULAR ACCESS PORT W/CATH. |
Classification | Port & Catheter, Implanted, Subcutaneous, Intravascular |
Applicant | STRATO MEDICAL CORP. 123 BRIMBAL AVE. P.O.B.3148 Beverly, MA 01915 |
Contact | Fenton, Jr. |
Correspondent | Fenton, Jr. 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 | 1988-01-25 |
Decision Date | 1988-04-26 |