The following data is part of a premarket notification filed by Strato Medical Corp. with the FDA for Strato Plast W/pre-attach Cath(lps 6015)/modified.
Device ID | K905851 |
510k Number | K905851 |
Device Name: | STRATO PLAST W/PRE-ATTACH CATH(LPS 6015)/MODIFIED |
Classification | Port & Catheter, Implanted, Subcutaneous, Intravascular |
Applicant | STRATO MEDICAL CORP. 123 BRIMBAL AVE. P.O.B.3148 Beverly, MA 01915 |
Contact | Nancy C Hall |
Correspondent | Nancy C Hall 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 | 1990-12-27 |
Decision Date | 1991-04-05 |