THE L-BOW ARM RESTRAINT
K-Number: K962778 · 1996-10-09
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Device Summary
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.
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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