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FDA 510(k)

THE L-BOW ARM RESTRAINT

K-Number: K962778 · 1996-10-09

ApplicantHeelbo, Inc.
Decision Date1996-10-09
Product CodeFMQ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

THE L-BOW ARM RESTRAINT is the device name listed in this FDA 510(k) record. The listed applicant is Heelbo, Inc.. It received FDA 510(k) clearance on 1996-10-09 under 510(k) number K962778. 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 THE L-BOW ARM RESTRAINT?

THE L-BOW ARM RESTRAINT is a medical device that received FDA 510(k) clearance on 1996-10-09. The listed applicant is Heelbo, Inc.. The 510(k) number is K962778.

When did THE L-BOW ARM RESTRAINT receive FDA 510(k) clearance?

THE L-BOW ARM RESTRAINT received FDA 510(k) clearance on 1996-10-09, under 510(k) number K962778.

Who is the listed applicant for THE L-BOW ARM RESTRAINT?

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

What is the FDA product code for THE L-BOW ARM RESTRAINT?

The FDA product code for THE L-BOW ARM 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 Heelbo, 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 14 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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