Cleared Traditional

13-220 TOW TYPES OF LEXER SCISSORS

K851757 · Artiberia · General & Plastic Surgery

Jun 1985

Decision

56d

Days

—

Risk

About This 510(k) Submission

K851757 is an FDA 510(k) clearance for the 13-220 TOW TYPES OF LEXER SCISSORS, 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 review panel.

Submission Details

510(k) Number	K851757 FDA.gov
FDA Decision	Cleared 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	—