PATIENT RESTRAINT SYSTEM
K-Number: K771659 · 1977-09-30
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Device Summary
Frequently Asked Questions
What is the PATIENT RESTRAINT SYSTEM?
PATIENT RESTRAINT SYSTEM is a medical device that received FDA 510(k) clearance on 1977-09-30. The listed applicant is Mtd, Inc.. The 510(k) number is K771659.
When did PATIENT RESTRAINT SYSTEM receive FDA 510(k) clearance?
PATIENT RESTRAINT SYSTEM received FDA 510(k) clearance on 1977-09-30, under 510(k) number K771659.
Who is the listed applicant for PATIENT RESTRAINT SYSTEM?
The FDA 510(k) record lists Mtd, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PATIENT RESTRAINT SYSTEM?
The FDA product code for PATIENT RESTRAINT SYSTEM 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 Mtd, 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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