MODEL R302DACS/A AUTOMATIC X-RAY COLLIMATOR
K-Number: K072780 · 2007-11-26
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Device Summary
Frequently Asked Questions
What is the MODEL R302DACS/A AUTOMATIC X-RAY COLLIMATOR?
MODEL R302DACS/A AUTOMATIC X-RAY COLLIMATOR is a medical device that received FDA 510(k) clearance on 2007-11-26. The listed applicant is Ralco S.R.L.. The 510(k) number is K072780.
When did MODEL R302DACS/A AUTOMATIC X-RAY COLLIMATOR receive FDA 510(k) clearance?
MODEL R302DACS/A AUTOMATIC X-RAY COLLIMATOR received FDA 510(k) clearance on 2007-11-26, under 510(k) number K072780.
Who is the listed applicant for MODEL R302DACS/A AUTOMATIC X-RAY COLLIMATOR?
The FDA 510(k) record lists Ralco S.R.L. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MODEL R302DACS/A AUTOMATIC X-RAY COLLIMATOR?
The FDA product code for MODEL R302DACS/A AUTOMATIC X-RAY COLLIMATOR is IZW.
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 Ralco S.R.L. 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: IZW)
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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