The following data is part of a premarket notification filed by Strato/infusaid, Inc. with the FDA for Strato/infusaid Infus-a-cath Dual Lumen Preattached Silicone Central Venous Catheter Systems.
Device ID | K953256 |
510k Number | K953256 |
Device Name: | STRATO/INFUSAID INFUS-A-CATH DUAL LUMEN PREATTACHED SILICONE CENTRAL VENOUS CATHETER SYSTEMS |
Classification | Catheter, Intravascular, Therapeutic, Long-term Greater Than 30 Days |
Applicant | STRATO/INFUSAID, INC. 1400 PROVIDENCE HIGHWAY Norwood, MA 02062 |
Contact | Craig M Audet |
Correspondent | Craig M Audet STRATO/INFUSAID, INC. 1400 PROVIDENCE HIGHWAY Norwood, MA 02062 |
Product Code | LJS |
CFR Regulation Number | 880.5970 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1995-07-12 |
Decision Date | 1995-10-04 |