The following data is part of a premarket notification filed by W.l. Gore & Associates,inc with the FDA for Diastat Vascular Access Graft.
Device ID | K955533 |
510k Number | K955533 |
Device Name: | DIASTAT VASCULAR ACCESS GRAFT |
Classification | Prosthesis, Vascular Graft, Of Less Then 6mm Diameter |
Applicant | W.L. GORE & ASSOCIATES,INC 1505 N. FOURTH ST. POB 2200 Flagstaff, AZ 86003 -2200 |
Contact | Timothy J Rynn |
Correspondent | Timothy J Rynn W.L. GORE & ASSOCIATES,INC 1505 N. FOURTH ST. POB 2200 Flagstaff, AZ 86003 -2200 |
Product Code | DYF |
CFR Regulation Number | 870.3450 [🔎] |
Decision | Se Subject To Tracking Reg (ST) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1995-12-05 |
Decision Date | 1996-05-15 |
Summary: | summary |