The following data is part of a premarket notification filed by Vascutech, Inc. with the FDA for Lemaitre Embolectomy Catheter.
Device ID | K992368 |
510k Number | K992368 |
Device Name: | LEMAITRE EMBOLECTOMY CATHETER |
Classification | Catheter, Embolectomy |
Applicant | VASCUTECH, INC. 164 MIDDLESEX TURNPIKE Burlington, MA 01803 |
Contact | Trent G Kamke |
Correspondent | Trent G Kamke VASCUTECH, INC. 164 MIDDLESEX TURNPIKE Burlington, MA 01803 |
Product Code | DXE |
CFR Regulation Number | 870.5150 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1999-07-15 |
Decision Date | 1999-12-09 |