Makrite Type N95 Respirator and Surgical Mask Model 910-N95

FDA 510(k) K020474 · Makrite Industries, Inc.

Substantially Equivalent

510(k) numberK020474

Submission

Device name
Makrite Type N95 Respirator and Surgical Mask Model 910-N95
Applicant
Makrite Industries, Inc.
Webster, MA, US
Received
February 12, 2002
Decision date
July 23, 2002
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
MSH – Respirator, Surgical
Device class
Class II (moderate risk)
Regulation
21 CFR 878.4040
Specialty
General, Plastic Surgery

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…

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K102923Barrier N95 Particulate RespiratorMSH · Abbreviated Molnlycke Health Care11/19/2010SE
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Questions and answers

When was Makrite Type N95 Respirator and Surgical Mask Model 910-N95 cleared by the FDA?

Makrite Type N95 Respirator and Surgical Mask Model 910-N95 (K020474) received a 510(k) decision of Substantially Equivalent on July 23, 2002, 161 days after the submission was received.

What is the product code of K020474?

The FDA product code is MSH – Respirator, Surgical, a Class II (moderate risk) device regulated under 21 CFR 878.4040.