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FDA 510(k)

BACK IN ACTION COMPRESSION & SUPPORT WITH MAGNETS FOR THE LOWER BACK, KNEE AND ANKLE

K-Number: K040054 · 2004-04-27

ApplicantTheodore Barash
Decision Date2004-04-27
Product CodeFQM
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

BACK IN ACTION COMPRESSION & SUPPORT WITH MAGNETS FOR THE LOWER BACK, KNEE AND ANKLE is the device name listed in this FDA 510(k) record. The listed applicant is Theodore Barash. It received FDA 510(k) clearance on 2004-04-27 under 510(k) number K040054. The device is classified under product code FQM. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BACK IN ACTION COMPRESSION & SUPPORT WITH MAGNETS FOR THE LOWER BACK, KNEE AND ANKLE?

BACK IN ACTION COMPRESSION & SUPPORT WITH MAGNETS FOR THE LOWER BACK, KNEE AND ANKLE is a medical device that received FDA 510(k) clearance on 2004-04-27. The listed applicant is Theodore Barash. The 510(k) number is K040054.

When did BACK IN ACTION COMPRESSION & SUPPORT WITH MAGNETS FOR THE LOWER BACK, KNEE AND ANKLE receive FDA 510(k) clearance?

BACK IN ACTION COMPRESSION & SUPPORT WITH MAGNETS FOR THE LOWER BACK, KNEE AND ANKLE received FDA 510(k) clearance on 2004-04-27, under 510(k) number K040054.

Who is the listed applicant for BACK IN ACTION COMPRESSION & SUPPORT WITH MAGNETS FOR THE LOWER BACK, KNEE AND ANKLE?

The FDA 510(k) record lists Theodore Barash as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BACK IN ACTION COMPRESSION & SUPPORT WITH MAGNETS FOR THE LOWER BACK, KNEE AND ANKLE?

The FDA product code for BACK IN ACTION COMPRESSION & SUPPORT WITH MAGNETS FOR THE LOWER BACK, KNEE AND ANKLE is FQM.

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Related Devices (Code: FQM)

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.

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Official Source

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

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