Cleared Traditional

K851753 - 13-100 TO 13-158 VARIOUS TYPES OF OPERATING SCISSO
(FDA 510(k) Clearance)

K851753 · Artiberia · General & Plastic Surgery device
Jun 1985
Decision
56d
Days
—
Risk

K851753 is an FDA 510(k) clearance for the 13-100 TO 13-158 VARIOUS TYPES OF OPERATING SCISSO..

Submitted by Artiberia (San Antonio, US). The FDA issued a Cleared decision on June 20, 1985, 56 days after receiving the submission on April 25, 1985.

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

Submission Details

510(k) Number K851753 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received April 25, 1985
Decision Date June 20, 1985
Days to Decision 56 days
Submission Type Traditional
Review Panel General & Plastic Surgery (SU)
Summary —

Device Classification

Product Code —
Device Class —