Cleared Traditional

SCISSORS

K823651 · Fred Sammons, Inc. · Physical Medicine
Feb 1983
Decision
59d
Days
Risk

About This 510(k) Submission

K823651 is an FDA 510(k) clearance for the SCISSORS, submitted by Fred Sammons, Inc. (Mchenry, US). The FDA issued a Cleared decision on February 3, 1983, 59 days after receiving the submission on December 6, 1982. This device falls under the Physical Medicine review panel.

Submission Details

510(k) Number K823651 FDA.gov
FDA Decision Cleared SESE
Date Received December 06, 1982
Decision Date February 03, 1983
Days to Decision 59 days
Submission Type Traditional
Review Panel Physical Medicine (PM)
Summary

Device Classification

Product Code
Device Class