ANKLE MOBILIZER
K-Number: K842882 · 1984-08-08
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Device Summary
Frequently Asked Questions
What is the ANKLE MOBILIZER?
ANKLE MOBILIZER is a medical device that received FDA 510(k) clearance on 1984-08-08. The listed applicant is Joint Mobilizer Systems, Inc.. The 510(k) number is K842882.
When did ANKLE MOBILIZER receive FDA 510(k) clearance?
ANKLE MOBILIZER received FDA 510(k) clearance on 1984-08-08, under 510(k) number K842882.
Who is the listed applicant for ANKLE MOBILIZER?
The FDA 510(k) record lists Joint Mobilizer Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ANKLE MOBILIZER?
The FDA product code for ANKLE MOBILIZER is BXB.
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 Joint Mobilizer Systems, 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.
Related Devices (Code: BXB)
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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