Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) 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

Decision Date2022-06-28
Product CodeFXX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

Magnum is the device name listed in this FDA 510(k) record. The listed applicant is Magnum Health and Safety Pvt, Ltd.. It received FDA 510(k) clearance on 2022-06-28 under 510(k) 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. The listed applicant is Magnum Health and Safety Pvt, Ltd.. The 510(k) number is K220670.

When did Magnum receive FDA 510(k) clearance?

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

Who is the listed applicant for Magnum?

The FDA 510(k) record lists Magnum Health and Safety Pvt, Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Magnum?

The FDA product code for Magnum is FXX.

Related Devices (Code: FXX)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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.