TORSO/WAIST RESTRAINT
K-Number: K963374 · 1996-11-08
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Device Summary
Frequently Asked Questions
What is the TORSO/WAIST RESTRAINT?
TORSO/WAIST RESTRAINT is a medical device that received FDA 510(k) clearance on 1996-11-08. The listed applicant is Morrison Medical Products. The 510(k) number is K963374.
When did TORSO/WAIST RESTRAINT receive FDA 510(k) clearance?
TORSO/WAIST RESTRAINT received FDA 510(k) clearance on 1996-11-08, under 510(k) number K963374.
Who is the listed applicant for TORSO/WAIST RESTRAINT?
The FDA 510(k) record lists Morrison Medical Products as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for TORSO/WAIST RESTRAINT?
The FDA product code for TORSO/WAIST 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 Morrison Medical Products 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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