The following data is part of a premarket notification filed by Intervascular, Inc. with the FDA for Intervascular Ochsner Micron Vascular Prostheses.
Device ID | K862739 |
510k Number | K862739 |
Device Name: | INTERVASCULAR OCHSNER MICRON VASCULAR PROSTHESES |
Classification | Prosthesis, Vascular Graft, Of 6mm And Greater Diameter |
Applicant | INTERVASCULAR, INC. 4906-A CREEKSIDE DR. Clearwater, FL 33520 |
Contact | Annette M Hillring |
Correspondent | Annette M Hillring INTERVASCULAR, INC. 4906-A CREEKSIDE DR. Clearwater, FL 33520 |
Product Code | DSY |
CFR Regulation Number | 870.3450 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1986-07-21 |
Decision Date | 1986-08-21 |