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FDA 510(k)

LEG PREP HOLDER

K-Number: K823391 · 1982-11-29

Decision Date1982-11-29
Product Code
DecisionSubstantially Equivalent

Device Summary

LEG PREP HOLDER is the device name listed in this FDA 510(k) record. The listed applicant is Orthopedic Systems, Inc.. It received FDA 510(k) clearance on 1982-11-29 under 510(k) number K823391. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LEG PREP HOLDER?

LEG PREP HOLDER is a medical device that received FDA 510(k) clearance on 1982-11-29. The listed applicant is Orthopedic Systems, Inc.. The 510(k) number is K823391.

When did LEG PREP HOLDER receive FDA 510(k) clearance?

LEG PREP HOLDER received FDA 510(k) clearance on 1982-11-29, under 510(k) number K823391.

Who is the listed applicant for LEG PREP HOLDER?

The FDA 510(k) record lists Orthopedic Systems, 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 Orthopedic Systems, 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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