Cleared Traditional

COMPLUS VARIOUS FORMS

K831039 · Parker Laboratories, Inc. · Dental
May 1983
Decision
57d
Days
Risk

About This 510(k) Submission

K831039 is an FDA 510(k) clearance for the COMPLUS VARIOUS FORMS, submitted by Parker Laboratories, Inc. (Mchenry, US). The FDA issued a Cleared decision on May 27, 1983, 57 days after receiving the submission on March 31, 1983. This device falls under the Dental review panel.

Submission Details

510(k) Number K831039 FDA.gov
FDA Decision Cleared SESE
Date Received March 31, 1983
Decision Date May 27, 1983
Days to Decision 57 days
Submission Type Traditional
Review Panel Dental (DE)
Summary

Device Classification

Product Code
Device Class