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FDA 510(k)

PELVIC WHEELCHAIR RESTRAINT

K-Number: K771715 · 1977-09-28

Decision Date1977-09-28
Product CodeFMQ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

PELVIC WHEELCHAIR RESTRAINT is the device name listed in this FDA 510(k) record. The listed applicant is Medical Restraints, Inc.. It received FDA 510(k) clearance on 1977-09-28 under 510(k) number K771715. 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 PELVIC WHEELCHAIR RESTRAINT?

PELVIC WHEELCHAIR RESTRAINT is a medical device that received FDA 510(k) clearance on 1977-09-28. The listed applicant is Medical Restraints, Inc.. The 510(k) number is K771715.

When did PELVIC WHEELCHAIR RESTRAINT receive FDA 510(k) clearance?

PELVIC WHEELCHAIR RESTRAINT received FDA 510(k) clearance on 1977-09-28, under 510(k) number K771715.

Who is the listed applicant for PELVIC WHEELCHAIR RESTRAINT?

The FDA 510(k) record lists Medical Restraints, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PELVIC WHEELCHAIR RESTRAINT?

The FDA product code for PELVIC WHEELCHAIR 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 Medical Restraints, 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.

View all 10 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

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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