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FDA 510(k)

FOOT DROP BOOT

K-Number: K771676 · 1977-09-20

Decision Date1977-09-20
Product CodeIQI
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

FOOT DROP BOOT is the device name listed in this FDA 510(k) record. The listed applicant is Medical Restraints, Inc.. It received FDA 510(k) clearance on 1977-09-20 under 510(k) number K771676. 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 FOOT DROP BOOT?

FOOT DROP BOOT is a medical device that received FDA 510(k) clearance on 1977-09-20. The listed applicant is Medical Restraints, Inc.. The 510(k) number is K771676.

When did FOOT DROP BOOT receive FDA 510(k) clearance?

FOOT DROP BOOT received FDA 510(k) clearance on 1977-09-20, under 510(k) number K771676.

Who is the listed applicant for FOOT DROP BOOT?

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

What is the FDA product code for FOOT DROP BOOT?

The FDA product code for FOOT DROP BOOT is IQI.

Other records listing Medical Restraints, 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.

View all 10 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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