THE HUESTIS COMPU-PLOTTER
K-Number: K901567 · 1990-05-31
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Device Summary
Frequently Asked Questions
What is the THE HUESTIS COMPU-PLOTTER?
THE HUESTIS COMPU-PLOTTER is a medical device that received FDA 510(k) clearance on 1990-05-31. The listed applicant is Huestis Machine Corp.. The 510(k) number is K901567.
When did THE HUESTIS COMPU-PLOTTER receive FDA 510(k) clearance?
THE HUESTIS COMPU-PLOTTER received FDA 510(k) clearance on 1990-05-31, under 510(k) number K901567.
Who is the listed applicant for THE HUESTIS COMPU-PLOTTER?
The FDA 510(k) record lists Huestis Machine Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for THE HUESTIS COMPU-PLOTTER?
The FDA product code for THE HUESTIS COMPU-PLOTTER is IXI.
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 Huestis Machine Corp. 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: IXI)
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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