Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR, NMPA) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

Magnum

K-Number: K220670 · 2022-06-28

ApplicantMagnum Health and Safety Pvt, Ltd.
Decision Date2022-06-28
Product CodeFXX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

Magnum is a medical device manufactured by Magnum Health and Safety Pvt, Ltd.. It received FDA 510(k) clearance on 2022-06-28 under approval number K220670. The device is classified under product code FXX. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Magnum?

Magnum is a medical device that received FDA 510(k) clearance on 2022-06-28. It is manufactured by Magnum Health and Safety Pvt, Ltd.. The 510(k) number is K220670.

When was Magnum approved by the FDA?

Magnum received FDA 510(k) clearance on 2022-06-28, under approval number K220670.

What company makes Magnum?

Magnum is manufactured by Magnum Health and Safety Pvt, Ltd..

What is the FDA product code for Magnum?

The FDA product code for Magnum is FXX.

Related Devices (Code: FXX)

K153409Protect U Guard Earloop and Tie-On Mask (Blue, White or Green)Protect U Guard, LLC K160269Surgical Face Masks (Ear loops and Tie-on)San-M Package Co., Ltd. K152197Skypro, SP01 MaskSkypro Medical Supplies Company K153496Disposable Surgical Face MaskXiantao Rayxin Medical Products Co., Ltd. K152561Communicator Surgical Facemask with Clear WindowPrestige Ameritech , Ltd. K171162Surgical Earloop Face Mask with Bottom Gap Shield and Surgical Tie-On Face Mask with Bottom Gap ShieldPrestige Ameritech

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

↑