Cleared Traditional

LIQUICORD

K092384 · Centrix, Inc. · Dental
Nov 2009
Decision
91d
Days
—
Risk

About This 510(k) Submission

K092384 is an FDA 510(k) clearance for the LIQUICORD, a Cord, Retraction, submitted by Centrix, Inc. (Shelton, US). The FDA issued a Cleared decision on November 4, 2009, 91 days after receiving the submission on August 5, 2009. This device falls under the Dental review panel.

Submission Details

510(k) Number K092384 FDA.gov
FDA Decision Cleared SESE
Date Received August 05, 2009
Decision Date November 04, 2009
Days to Decision 91 days
Submission Type Traditional
Review Panel Dental (DE)
Summary Statement

Device Classification

Product Code MVL — Cord, Retraction
Device Class —