KINESETHETIC SEATING SYSTEM/WHEELCHAIR
K-Number: K861754 · 1986-05-23
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Device Summary
Frequently Asked Questions
What is the KINESETHETIC SEATING SYSTEM/WHEELCHAIR?
KINESETHETIC SEATING SYSTEM/WHEELCHAIR is a medical device that received FDA 510(k) clearance on 1986-05-23. The listed applicant is Special Health Systems, Ltd.. The 510(k) number is K861754.
When did KINESETHETIC SEATING SYSTEM/WHEELCHAIR receive FDA 510(k) clearance?
KINESETHETIC SEATING SYSTEM/WHEELCHAIR received FDA 510(k) clearance on 1986-05-23, under 510(k) number K861754.
Who is the listed applicant for KINESETHETIC SEATING SYSTEM/WHEELCHAIR?
The FDA 510(k) record lists Special Health Systems, Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for KINESETHETIC SEATING SYSTEM/WHEELCHAIR?
The FDA product code for KINESETHETIC SEATING SYSTEM/WHEELCHAIR is KNN.
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 Special Health Systems, Ltd. 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: KNN)
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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