SUPPORT VEST
K-Number: K963459 · 1996-10-15
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Device Summary
Frequently Asked Questions
What is the SUPPORT VEST?
SUPPORT VEST is a medical device that received FDA 510(k) clearance on 1996-10-15. The listed applicant is Skil-Care Corp.. The 510(k) number is K963459.
When did SUPPORT VEST receive FDA 510(k) clearance?
SUPPORT VEST received FDA 510(k) clearance on 1996-10-15, under 510(k) number K963459.
Who is the listed applicant for SUPPORT VEST?
The FDA 510(k) record lists Skil-Care Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SUPPORT VEST?
The FDA product code for SUPPORT VEST 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 Skil-Care Corp. 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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