Cleared Traditional

SUTURE TRAY

K843525 · Pro-Lab, Inc. · General & Plastic Surgery

Nov 1984

Decision

59d

Days

—

Risk

About This 510(k) Submission

K843525 is an FDA 510(k) clearance for the SUTURE TRAY, submitted by Pro-Lab, Inc. (Round Rock, US). The FDA issued a Cleared decision on November 5, 1984, 59 days after receiving the submission on September 7, 1984. This device falls under the General & Plastic Surgery review panel.

Submission Details

510(k) Number	K843525 FDA.gov
FDA Decision	Cleared SESE
Date Received	September 07, 1984
Decision Date	November 05, 1984
Days to Decision	59 days
Submission Type	Traditional
Review Panel	General & Plastic Surgery (SU)
Summary	—