The following data is part of a premarket notification filed by Lake Region Mfg., Inc. with the FDA for Cardiovascular And Vascular Guidewire Modifications.
Device ID | K935170 |
510k Number | K935170 |
Device Name: | CARDIOVASCULAR AND VASCULAR GUIDEWIRE MODIFICATIONS |
Classification | Wire, Guide, Catheter |
Applicant | LAKE REGION MFG., INC. 340 LAKE HAZELTINE DR. Chaska, MN 55318 |
Contact | Carl Beaurline |
Correspondent | Carl Beaurline LAKE REGION MFG., INC. 340 LAKE HAZELTINE DR. Chaska, MN 55318 |
Product Code | DQX |
CFR Regulation Number | 870.1330 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1993-10-27 |
Decision Date | 1994-03-31 |