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FDA 510(k)

SUPPORT VEST

K-Number: K963459 · 1996-10-15

Decision Date1996-10-15
Product CodeKID
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

SUPPORT VEST is the device name listed in this FDA 510(k) record. The listed applicant is Skil-Care Corp.. It received FDA 510(k) clearance on 1996-10-15 under 510(k) number K963459. The device is classified under product code KID. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

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.

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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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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