The following data is part of a premarket notification filed by Meadox Medicals, Div. Boston Scientific Corp. with the FDA for Meados Intraortic Graft.
Device ID | K841596 |
510k Number | K841596 |
Device Name: | MEADOS INTRAORTIC GRAFT |
Classification | Prosthesis, Vascular Graft, Of 6mm And Greater Diameter |
Applicant | MEADOX MEDICALS, DIV. BOSTON SCIENTIFIC CORP. 103 BAUER DR. P.O. BOX 530 Oakland, NJ 07436 |
Contact | Scott Mindrebo |
Correspondent | Scott Mindrebo MEADOX MEDICALS, DIV. BOSTON SCIENTIFIC CORP. 103 BAUER DR. P.O. BOX 530 Oakland, NJ 07436 |
Product Code | DSY |
CFR Regulation Number | 870.3450 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1984-04-18 |
Decision Date | 1986-05-08 |