The following data is part of a premarket notification filed by Strato Medical Corp. with the FDA for Strato Medical Infuse-a-cath, Triple Lumen Polyurethane, Central Vnous Catheter Systems.
Device ID | K946250 |
510k Number | K946250 |
Device Name: | STRATO MEDICAL INFUSE-A-CATH, TRIPLE LUMEN POLYURETHANE, CENTRAL VNOUS CATHETER SYSTEMS |
Classification | Catheter, Intravascular, Therapeutic, Long-term Greater Than 30 Days |
Applicant | STRATO MEDICAL CORP. 123 BRIMBAL AVE. Beverly, MA 01915 -1892 |
Contact | Craig M Audet |
Correspondent | Craig M Audet STRATO MEDICAL CORP. 123 BRIMBAL AVE. Beverly, MA 01915 -1892 |
Product Code | LJS |
CFR Regulation Number | 880.5970 [🔎] |
Decision | Substantially Equivalent - Kit (SESK) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1994-12-23 |
Decision Date | 1995-05-02 |