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FDA 510(k)

MASTERFOOT CAST HEEL

K-Number: K840617 · 1984-03-23

ApplicantSeton Products, Inc.
Decision Date1984-03-23
Product CodeLGF
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

MASTERFOOT CAST HEEL is the device name listed in this FDA 510(k) record. The listed applicant is Seton Products, Inc.. It received FDA 510(k) clearance on 1984-03-23 under 510(k) number K840617. 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 MASTERFOOT CAST HEEL?

MASTERFOOT CAST HEEL is a medical device that received FDA 510(k) clearance on 1984-03-23. The listed applicant is Seton Products, Inc.. The 510(k) number is K840617.

When did MASTERFOOT CAST HEEL receive FDA 510(k) clearance?

MASTERFOOT CAST HEEL received FDA 510(k) clearance on 1984-03-23, under 510(k) number K840617.

Who is the listed applicant for MASTERFOOT CAST HEEL?

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

What is the FDA product code for MASTERFOOT CAST HEEL?

The FDA product code for MASTERFOOT CAST HEEL is LGF.

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Other records listing Seton Products, Inc. as applicant

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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.

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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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