The following data is part of a premarket notification filed by Micrus Endovascular Corporation with the FDA for Micrus Microcatheter, Model Courier 270.
| Device ID | K092702 |
| 510k Number | K092702 |
| Device Name: | MICRUS MICROCATHETER, MODEL COURIER 270 |
| Classification | Catheter, Intravascular, Diagnostic |
| Applicant | MICRUS ENDOVASCULAR CORPORATION 821 FOX LANE San Jose, CA 95131 |
| Contact | Patrick Lee |
| Correspondent | Patrick Lee MICRUS ENDOVASCULAR CORPORATION 821 FOX LANE San Jose, CA 95131 |
| Product Code | DQO |
| CFR Regulation Number | 870.1200 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2009-09-02 |
| Decision Date | 2009-11-20 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 00878528009078 | K092702 | 000 |