TUXEDO VEST RESTRAINT
K-Number: K963474 · 1997-01-22
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Device Summary
Frequently Asked Questions
What is the TUXEDO VEST RESTRAINT?
TUXEDO VEST RESTRAINT is a medical device that received FDA 510(k) clearance on 1997-01-22. The listed applicant is Deroyal Industries, Inc.. The 510(k) number is K963474.
When did TUXEDO VEST RESTRAINT receive FDA 510(k) clearance?
TUXEDO VEST RESTRAINT received FDA 510(k) clearance on 1997-01-22, under 510(k) number K963474.
Who is the listed applicant for TUXEDO 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 TUXEDO VEST RESTRAINT?
The FDA product code for TUXEDO 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.
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
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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