.DECIMAL ELECTRON APERTURE
K-Number: K111759 · 2011-09-09
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Device Summary
Frequently Asked Questions
What is the .DECIMAL ELECTRON APERTURE?
.DECIMAL ELECTRON APERTURE is a medical device that received FDA 510(k) clearance on 2011-09-09. The listed applicant is .Decimal, Inc.. The 510(k) number is K111759.
When did .DECIMAL ELECTRON APERTURE receive FDA 510(k) clearance?
.DECIMAL ELECTRON APERTURE received FDA 510(k) clearance on 2011-09-09, under 510(k) number K111759.
Who is the listed applicant for .DECIMAL ELECTRON APERTURE?
The FDA 510(k) record lists .Decimal, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for .DECIMAL ELECTRON APERTURE?
The FDA product code for .DECIMAL ELECTRON APERTURE 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 .Decimal, 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: 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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