Cleared Traditional

K854339 - CUI CHIN SIZER
(FDA 510(k) Clearance)

K854339 · Cox-Uphuff Intl. · General & Plastic Surgery device
Nov 1985
Decision
18d
Days
—
Risk

K854339 is an FDA 510(k) clearance for the CUI CHIN SIZER..

Submitted by Cox-Uphuff Intl. (Santa Barbara, US). The FDA issued a Cleared decision on November 15, 1985, 18 days after receiving the submission on October 28, 1985.

This device falls under the General & Plastic Surgery FDA review panel.

Submission Details

510(k) Number K854339 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received October 28, 1985
Decision Date November 15, 1985
Days to Decision 18 days
Submission Type Traditional
Review Panel General & Plastic Surgery (SU)
Summary —

Device Classification

Product Code —
Device Class —