HUESTIS COMPU-FORMER
K-Number: K880047 · 1988-04-11
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Device Summary
Frequently Asked Questions
What is the HUESTIS COMPU-FORMER?
HUESTIS COMPU-FORMER is a medical device that received FDA 510(k) clearance on 1988-04-11. The listed applicant is Huestis Machine Corp.. The 510(k) number is K880047.
When did HUESTIS COMPU-FORMER receive FDA 510(k) clearance?
HUESTIS COMPU-FORMER received FDA 510(k) clearance on 1988-04-11, under 510(k) number K880047.
Who is the listed applicant for HUESTIS COMPU-FORMER?
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 HUESTIS COMPU-FORMER?
The FDA product code for HUESTIS COMPU-FORMER 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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