Liquicord
510(k) K092384
Liquicord is a medical device (FDA unclassified; FDA product code MVL, Cord, Retraction) made by Centrix, Inc., cleared under FDA 510(k) K092384 on 4 Nov 2009, active as of 22 Oct 2026.
Active
510(k)
Valid until
No expiry
FDA recalls
None found
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | FDA 510(k)SESE | NumberK092384 | Date4 Nov 2009 | StatusActive |
Official records
- FDA 510(k) database K092384
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- 510(k) Number
- FDA product code
- MVL
- Device class
- U
- Advisory committee
- Unknown
- FDA decision
- SESE Substantially Equivalent
Similar devices
Other devices filed under FDA product code MVL (Cord, Retraction).
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