GAIT-AID ORTHOPEDIC INSOLE
K-Number: K874502 · 1987-11-30
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Device Summary
Frequently Asked Questions
What is the GAIT-AID ORTHOPEDIC INSOLE?
GAIT-AID ORTHOPEDIC INSOLE is a medical device that received FDA 510(k) clearance on 1987-11-30. The listed applicant is Gait-Aid, Inc.. The 510(k) number is K874502.
When did GAIT-AID ORTHOPEDIC INSOLE receive FDA 510(k) clearance?
GAIT-AID ORTHOPEDIC INSOLE received FDA 510(k) clearance on 1987-11-30, under 510(k) number K874502.
Who is the listed applicant for GAIT-AID ORTHOPEDIC INSOLE?
The FDA 510(k) record lists Gait-Aid, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for GAIT-AID ORTHOPEDIC INSOLE?
The FDA product code for GAIT-AID ORTHOPEDIC INSOLE 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.
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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