Cleared Traditional

K062795 - MUGARD MUCOADHESIVE ORAL WOUND RINSE
(FDA 510(k) Clearance)

Dec 2006
Decision
84d
Days
Risk

K062795 is an FDA 510(k) clearance for the MUGARD MUCOADHESIVE ORAL WOUND RINSE. This device is classified as a Oral Wound Dressing.

Submitted by Access Pharmaceuticals, Inc. (Dallas, US). The FDA issued a Cleared decision on December 11, 2006, 84 days after receiving the submission on September 18, 2006.

This device falls under the General & Plastic Surgery FDA review panel. Intended As A Physical Barrier For Temporary Protection Of Oral Mucosal Tissue And To Provide Pain Relief. Unclassified Status Per Se To Mgq..

Submission Details

510(k) Number K062795 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received September 18, 2006
Decision Date December 11, 2006
Days to Decision 84 days
Submission Type Traditional
Review Panel General & Plastic Surgery (SU)
Summary Summary PDF

Device Classification

Product Code OLR — Oral Wound Dressing
Device Class
Definition Intended As A Physical Barrier For Temporary Protection Of Oral Mucosal Tissue And To Provide Pain Relief. Unclassified Status Per Se To Mgq.