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FDA 510(k)

FORMED STEEL DEVICE KEEP LEGS SEPARATED

K-Number: K823629 · 1982-12-30

Decision Date1982-12-30
Product Code
DecisionSubstantially Equivalent

Device Summary

FORMED STEEL DEVICE KEEP LEGS SEPARATED is the device name listed in this FDA 510(k) record. The listed applicant is Fred Sammons, Inc.. It received FDA 510(k) clearance on 1982-12-30 under 510(k) number K823629. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FORMED STEEL DEVICE KEEP LEGS SEPARATED?

FORMED STEEL DEVICE KEEP LEGS SEPARATED is a medical device that received FDA 510(k) clearance on 1982-12-30. The listed applicant is Fred Sammons, Inc.. The 510(k) number is K823629.

When did FORMED STEEL DEVICE KEEP LEGS SEPARATED receive FDA 510(k) clearance?

FORMED STEEL DEVICE KEEP LEGS SEPARATED received FDA 510(k) clearance on 1982-12-30, under 510(k) number K823629.

Who is the listed applicant for FORMED STEEL DEVICE KEEP LEGS SEPARATED?

The FDA 510(k) record lists Fred Sammons, Inc. as the applicant. This does not by itself establish the device manufacturer.

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 Fred Sammons, Inc. 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.

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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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