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FDA 510(k)

PEDESTAL WALKING HEEL PRODUCT NO. 4183-133

K-Number: K873722 · 1987-10-02

Decision Date1987-10-02
Product CodeLGF
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

PEDESTAL WALKING HEEL PRODUCT NO. 4183-133 is the device name listed in this FDA 510(k) record. The listed applicant is Martin Medical. It received FDA 510(k) clearance on 1987-10-02 under 510(k) number K873722. The device is classified under product code LGF. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PEDESTAL WALKING HEEL PRODUCT NO. 4183-133?

PEDESTAL WALKING HEEL PRODUCT NO. 4183-133 is a medical device that received FDA 510(k) clearance on 1987-10-02. The listed applicant is Martin Medical. The 510(k) number is K873722.

When did PEDESTAL WALKING HEEL PRODUCT NO. 4183-133 receive FDA 510(k) clearance?

PEDESTAL WALKING HEEL PRODUCT NO. 4183-133 received FDA 510(k) clearance on 1987-10-02, under 510(k) number K873722.

Who is the listed applicant for PEDESTAL WALKING HEEL PRODUCT NO. 4183-133?

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

What is the FDA product code for PEDESTAL WALKING HEEL PRODUCT NO. 4183-133?

The FDA product code for PEDESTAL WALKING HEEL PRODUCT NO. 4183-133 is LGF.

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 Martin Medical 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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Related Devices (Code: LGF)

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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