REMREST
K-Number: K002763 · 2001-05-04
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Device Summary
Frequently Asked Questions
What is the REMREST?
REMREST is a medical device that received FDA 510(k) clearance on 2001-05-04. The listed applicant is Medical Industries America, Inc.. The 510(k) number is K002763.
When did REMREST receive FDA 510(k) clearance?
REMREST received FDA 510(k) clearance on 2001-05-04, under 510(k) number K002763.
Who is the listed applicant for REMREST?
The FDA 510(k) record lists Medical Industries America, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for REMREST?
The FDA product code for REMREST is BZD.
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 Industries America, 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: BZD)
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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