LIQUICORD
Cord, Retraction
CENTRIX, INC.
The following data is part of a premarket notification filed by Centrix, Inc. with the FDA for Liquicord.
Pre-market Notification Details
| Device ID | K092384 |
| 510k Number | K092384 |
| Device Name: | LIQUICORD |
| Classification | Cord, Retraction |
| Applicant | CENTRIX, INC. 770 RIVER RD. Shelton, CT 06484 -5458 |
| Contact | Roger Mastrony |
| Correspondent | Roger Mastrony CENTRIX, INC. 770 RIVER RD. Shelton, CT 06484 -5458 |
| Product Code | MVL |
| CFR Regulation Number | 510(k) Premarket Notification [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2009-08-05 |
| Decision Date | 2009-11-04 |
Trademark Results [LIQUICORD]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 LIQUICORD 88273211 not registered Live/Pending |
S & C Polymer Silicon- und Composite Spezialitäten GmbH 2019-01-23 |
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