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FDA 510(k)

DROP FOOT BRACE

K-Number: K831615 · 1983-06-15

ApplicantEdward Dilauro, Jr.
Decision Date1983-06-15
Product CodeIQI
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

DROP FOOT BRACE is the device name listed in this FDA 510(k) record. The listed applicant is Edward Dilauro, Jr.. It received FDA 510(k) clearance on 1983-06-15 under 510(k) number K831615. 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 DROP FOOT BRACE?

DROP FOOT BRACE is a medical device that received FDA 510(k) clearance on 1983-06-15. The listed applicant is Edward Dilauro, Jr.. The 510(k) number is K831615.

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

DROP FOOT BRACE received FDA 510(k) clearance on 1983-06-15, under 510(k) number K831615.

Who is the listed applicant for DROP FOOT BRACE?

The FDA 510(k) record lists Edward Dilauro, Jr. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DROP FOOT BRACE?

The FDA product code for DROP FOOT BRACE is IQI.

Related Clinical Trials

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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.

K052771SENSOR WALKOtto Bock Healthcare LPK031576SPARTAN ORTHOPAEDIC WRIST BRACE, MODEL SCT-1Surgitech, Inc.K926391ACCUFLEX DYNAMIC ELBOW ORTHOSISRegulatory & Marketing Services, Inc.K910974MCCONNELL SHOULDER BRACEMcconnell OrthopedicK874502GAIT-AID ORTHOPEDIC INSOLEGait-Aid, Inc.K831542ADJUSTABLE POLYCENTRIC ELBOW HINGEFred Sammons, Inc.

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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