The following data is part of a premarket notification filed by Enroxtech, Inc. with the FDA for Endo-cord.
Device ID | K141330 |
510k Number | K141330 |
Device Name: | ENDO-CORD |
Classification | Light, Surgical, Fiberoptic |
Applicant | ENROXTECH, INC. 4655 KIRKWOOD COURT Boulder, CO 80301 |
Contact | Lewis Ward |
Correspondent | Lewis Ward ENROXTECH, INC. 4655 KIRKWOOD COURT Boulder, CO 80301 |
Product Code | FST |
CFR Regulation Number | 878.4580 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2014-05-21 |
Decision Date | 2014-12-15 |
Summary: | summary |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() ENDO-CORD 85663377 not registered Dead/Abandoned |
EnroxTech, Inc. 2012-06-27 |