ENDO-CORD
Light, Surgical, Fiberoptic
ENROXTECH, INC.
The following data is part of a premarket notification filed by Enroxtech, Inc. with the FDA for Endo-cord.
Pre-market Notification Details
| 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 |
Trademark Results [ENDO-CORD]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 ENDO-CORD 85663377 not registered Dead/Abandoned |
EnroxTech, Inc. 2012-06-27 |
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