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FDA 510(k)

LOWER EXTREMITY SUPPORT SYSTEM-LESS

K-Number: K810433 · 1981-03-13

Decision Date1981-03-13
Product CodeFWZ
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

LOWER EXTREMITY SUPPORT SYSTEM-LESS is the device name listed in this FDA 510(k) record. The listed applicant is Walgen Medical Innoventions. It received FDA 510(k) clearance on 1981-03-13 under 510(k) number K810433. The device is classified under product code FWZ. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LOWER EXTREMITY SUPPORT SYSTEM-LESS?

LOWER EXTREMITY SUPPORT SYSTEM-LESS is a medical device that received FDA 510(k) clearance on 1981-03-13. The listed applicant is Walgen Medical Innoventions. The 510(k) number is K810433.

When did LOWER EXTREMITY SUPPORT SYSTEM-LESS receive FDA 510(k) clearance?

LOWER EXTREMITY SUPPORT SYSTEM-LESS received FDA 510(k) clearance on 1981-03-13, under 510(k) number K810433.

Who is the listed applicant for LOWER EXTREMITY SUPPORT SYSTEM-LESS?

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

What is the FDA product code for LOWER EXTREMITY SUPPORT SYSTEM-LESS?

The FDA product code for LOWER EXTREMITY SUPPORT SYSTEM-LESS is FWZ.

Related Clinical Trials

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.

Other records listing Walgen Medical Innoventions as applicant

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.

Related Devices (Code: FWZ)

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

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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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