The following data is part of a premarket notification filed by Micro Therapeutics, Inc. with the FDA for Echelon Micro Catheter, Model 105-5092-150.
Device ID | K030688 |
510k Number | K030688 |
Device Name: | ECHELON MICRO CATHETER, MODEL 105-5092-150 |
Classification | Catheter, Continuous Flush |
Applicant | MICRO THERAPEUTICS, INC. 2 GOODYEAR Irvine, CA 92618 |
Contact | Marilyn R Pourazar |
Correspondent | Marilyn R Pourazar MICRO THERAPEUTICS, INC. 2 GOODYEAR Irvine, CA 92618 |
Product Code | KRA |
CFR Regulation Number | 870.1210 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Special |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2003-03-05 |
Decision Date | 2003-03-28 |
Summary: | summary |