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FDA 510(k)

PEDIATRIC VEST RESTRAINT

K-Number: K963472 · 1996-11-14

Decision Date1996-11-14
Product CodeFMQ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

PEDIATRIC VEST RESTRAINT is the device name listed in this FDA 510(k) record. The listed applicant is Deroyal Industries, Inc.. It received FDA 510(k) clearance on 1996-11-14 under 510(k) number K963472. 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 PEDIATRIC VEST RESTRAINT?

PEDIATRIC VEST RESTRAINT is a medical device that received FDA 510(k) clearance on 1996-11-14. The listed applicant is Deroyal Industries, Inc.. The 510(k) number is K963472.

When did PEDIATRIC VEST RESTRAINT receive FDA 510(k) clearance?

PEDIATRIC VEST RESTRAINT received FDA 510(k) clearance on 1996-11-14, under 510(k) number K963472.

Who is the listed applicant for PEDIATRIC VEST RESTRAINT?

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 PEDIATRIC VEST RESTRAINT?

The FDA product code for PEDIATRIC VEST RESTRAINT 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 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.

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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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