WHEELCHAIR BELT
K-Number: K963479 · 1997-01-24
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Device Summary
Frequently Asked Questions
What is the WHEELCHAIR BELT?
WHEELCHAIR BELT is a medical device that received FDA 510(k) clearance on 1997-01-24. The listed applicant is Deroyal Industries, Inc.. The 510(k) number is K963479.
When did WHEELCHAIR BELT receive FDA 510(k) clearance?
WHEELCHAIR BELT received FDA 510(k) clearance on 1997-01-24, under 510(k) number K963479.
Who is the listed applicant for WHEELCHAIR BELT?
The FDA 510(k) record lists Deroyal Industries, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for WHEELCHAIR BELT?
The FDA product code for WHEELCHAIR BELT is KID.
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 Deroyal Industries, 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: KID)
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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