REST ASSURED NITE PROTECTOR
K-Number: K063229 · 2006-12-19
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Device Summary
Frequently Asked Questions
What is the REST ASSURED NITE PROTECTOR?
REST ASSURED NITE PROTECTOR is a medical device that received FDA 510(k) clearance on 2006-12-19. The listed applicant is Ranir, LLC. The 510(k) number is K063229.
When did REST ASSURED NITE PROTECTOR receive FDA 510(k) clearance?
REST ASSURED NITE PROTECTOR received FDA 510(k) clearance on 2006-12-19, under 510(k) number K063229.
Who is the listed applicant for REST ASSURED NITE PROTECTOR?
The FDA 510(k) record lists Ranir, LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for REST ASSURED NITE PROTECTOR?
The FDA product code for REST ASSURED NITE PROTECTOR is OBR. This falls under the Orthopedic category.
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 Ranir, LLC 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: OBR)
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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