PATIENT POSITIONING SYSTEM 1D OR 2D
K-Number: K800223 · 1980-03-03
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Device Summary
Frequently Asked Questions
What is the PATIENT POSITIONING SYSTEM 1D OR 2D?
PATIENT POSITIONING SYSTEM 1D OR 2D is a medical device that received FDA 510(k) clearance on 1980-03-03. The listed applicant is Laboratoire National D'Essais. The 510(k) number is K800223.
When did PATIENT POSITIONING SYSTEM 1D OR 2D receive FDA 510(k) clearance?
PATIENT POSITIONING SYSTEM 1D OR 2D received FDA 510(k) clearance on 1980-03-03, under 510(k) number K800223.
Who is the listed applicant for PATIENT POSITIONING SYSTEM 1D OR 2D?
The FDA 510(k) record lists Laboratoire National D'Essais as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PATIENT POSITIONING SYSTEM 1D OR 2D?
The FDA product code for PATIENT POSITIONING SYSTEM 1D OR 2D is IWE.
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.
Related Devices (Code: IWE)
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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