The following data is part of a premarket notification filed by William Cook Europe Aps with the FDA for Lunderquist Extra Stiff Wire Guide.
Device ID | K171513 |
510k Number | K171513 |
Device Name: | Lunderquist Extra Stiff Wire Guide |
Classification | Wire, Guide, Catheter |
Applicant | William Cook Europe ApS Sandet 6 Bjaeverskov, DK 4632 |
Contact | Henriette Stordal Christiansen |
Correspondent | Henriette Stordal Christiansen William Cook Europe ApS Sandet 6 Bjaeverskov, DK 4632 |
Product Code | DQX |
CFR Regulation Number | 870.1330 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2017-05-24 |
Decision Date | 2017-12-07 |
Summary: | summary |