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FDA 510(k)

OHC DYNAMIC CLUB FOOT BRACE

K-Number: K800715 · 1980-05-02

ApplicantIpos Luneburg
Decision Date1980-05-02
Product CodeIQI
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

OHC DYNAMIC CLUB FOOT BRACE is the device name listed in this FDA 510(k) record. The listed applicant is Ipos Luneburg. It received FDA 510(k) clearance on 1980-05-02 under 510(k) number K800715. The device is classified under product code IQI. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OHC DYNAMIC CLUB FOOT BRACE?

OHC DYNAMIC CLUB FOOT BRACE is a medical device that received FDA 510(k) clearance on 1980-05-02. The listed applicant is Ipos Luneburg. The 510(k) number is K800715.

When did OHC DYNAMIC CLUB FOOT BRACE receive FDA 510(k) clearance?

OHC DYNAMIC CLUB FOOT BRACE received FDA 510(k) clearance on 1980-05-02, under 510(k) number K800715.

Who is the listed applicant for OHC DYNAMIC CLUB FOOT BRACE?

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

What is the FDA product code for OHC DYNAMIC CLUB FOOT BRACE?

The FDA product code for OHC DYNAMIC CLUB FOOT BRACE is IQI.

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 Ipos Luneburg 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.

View all 8 devices →

Related Devices (Code: IQI)

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.

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