ANKLE RESTRAINT SYSTEM
K-Number: K963416 · 1996-11-06
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Device Summary
Frequently Asked Questions
What is the ANKLE RESTRAINT SYSTEM?
ANKLE RESTRAINT SYSTEM is a medical device that received FDA 510(k) clearance on 1996-11-06. The listed applicant is Morrison Medical Products. The 510(k) number is K963416.
When did ANKLE RESTRAINT SYSTEM receive FDA 510(k) clearance?
ANKLE RESTRAINT SYSTEM received FDA 510(k) clearance on 1996-11-06, under 510(k) number K963416.
Who is the listed applicant for ANKLE RESTRAINT SYSTEM?
The FDA 510(k) record lists Morrison Medical Products as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ANKLE RESTRAINT SYSTEM?
The FDA product code for ANKLE RESTRAINT SYSTEM is FMQ.
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 Morrison Medical Products 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.
Related Devices (Code: FMQ)
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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