Cleared Traditional

I/A PROBE LINES

K834577 · Frigitronics of Connecticut, Inc. · General & Plastic Surgery
May 1984
Decision
145d
Days
Risk

About This 510(k) Submission

K834577 is an FDA 510(k) clearance for the I/A PROBE LINES, submitted by Frigitronics of Connecticut, Inc. (Walker, US). The FDA issued a Cleared decision on May 22, 1984, 145 days after receiving the submission on December 29, 1983. This device falls under the General & Plastic Surgery review panel.

Submission Details

510(k) Number K834577 FDA.gov
FDA Decision Cleared SESE
Date Received December 29, 1983
Decision Date May 22, 1984
Days to Decision 145 days
Submission Type Traditional
Review Panel General & Plastic Surgery (SU)
Summary

Device Classification

Product Code
Device Class