Cleared Traditional

Master-Frank N95 Particulate Respirator

K172963 · Master & Frank Enterprise Co., Ltd. · General Hospital

Apr 2018

Decision

190d

Days

Class 2

Risk

About This 510(k) Submission

K172963 is an FDA 510(k) clearance for the Master-Frank N95 Particulate Respirator, a Respirator, Surgical (Class II — Special Controls, product code MSH), submitted by Master & Frank Enterprise Co., Ltd. (Dong Duan, CN). The FDA issued a Cleared decision on April 4, 2018, 190 days after receiving the submission on September 26, 2017. This device falls under the General Hospital review panel. Regulated under 21 CFR 878.4040.

Submission Details

510(k) Number	K172963 FDA.gov
FDA Decision	Cleared SESE
Date Received	September 26, 2017
Decision Date	April 04, 2018
Days to Decision	190 days
Submission Type	Traditional
Review Panel	General Hospital (HO)
Summary	Summary PDF

Device Classification

Product Code	MSH — Respirator, Surgical
Device Class	Class II — Special Controls
CFR Regulation	21 CFR 878.4040
Definition	A Surgical N95 Respirator Or N95 Filtering Facepiece Respirator Is Not Exempt If It Is Intended To Prevent Specific Diseases Or Infections, Or It Is Labeled Or Otherwise Represented As Filtering Surgical Smoke Or Plumes, Filtering Specific Amounts Of Viruses Or Bacteria, Reducing The Amount Of And/or Killing Viruses, Bacteria, Or Fungi, Or Affecting Allergenicity, Or It Contains�coating Technologies Unrelated To Filtration (e.g., To Reduce And Or Kill Microorganisms).��surgical N95 Respirators And N95 Filtering Facepiece Respirators Are Exempt From The Premarket Notification Procedures Subject To 21 Cfr 878.9 And The Conditions For Exemption Identified In 21 Cfr 878.4040(b)(1).