The following data is part of a premarket notification filed by Micro Therapeutics, Inc. with the FDA for Marathon Flow Directed Micro Catheter, Model 105-5055.
Device ID | K034036 |
510k Number | K034036 |
Device Name: | MARATHON FLOW DIRECTED MICRO CATHETER, MODEL 105-5055 |
Classification | Catheter, Continuous Flush |
Applicant | MICRO THERAPEUTICS, INC. 2 GOODYEAR Irvine, CA 92618 |
Contact | Bill Hyatt |
Correspondent | Bill Hyatt MICRO THERAPEUTICS, INC. 2 GOODYEAR Irvine, CA 92618 |
Product Code | KRA |
CFR Regulation Number | 870.1210 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2003-12-29 |
Decision Date | 2004-02-13 |
Summary: | summary |