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FDA 510(k)

DOUBLE SUPPORT PONCHO/SLIDER PONCHO

K-Number: K963447 · 1996-10-07

Decision Date1996-10-07
Product CodeFMQ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

DOUBLE SUPPORT PONCHO/SLIDER PONCHO 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 1996-10-07 under 510(k) number K963447. The device is classified under product code FMQ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DOUBLE SUPPORT PONCHO/SLIDER PONCHO?

DOUBLE SUPPORT PONCHO/SLIDER PONCHO is a medical device that received FDA 510(k) clearance on 1996-10-07. The listed applicant is Skil-Care Corp.. The 510(k) number is K963447.

When did DOUBLE SUPPORT PONCHO/SLIDER PONCHO receive FDA 510(k) clearance?

DOUBLE SUPPORT PONCHO/SLIDER PONCHO received FDA 510(k) clearance on 1996-10-07, under 510(k) number K963447.

Who is the listed applicant for DOUBLE SUPPORT PONCHO/SLIDER PONCHO?

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 DOUBLE SUPPORT PONCHO/SLIDER PONCHO?

The FDA product code for DOUBLE SUPPORT PONCHO/SLIDER PONCHO is FMQ.

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.

View all 20 devices →

Related Devices (Code: FMQ)

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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