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FDA 510(k)

MODEL R302DACS/A AUTOMATIC X-RAY COLLIMATOR

K-Number: K072780 · 2007-11-26

ApplicantRalco S.R.L.
Decision Date2007-11-26
Product CodeIZW
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MODEL R302DACS/A AUTOMATIC X-RAY COLLIMATOR is the device name listed in this FDA 510(k) record. The listed applicant is Ralco S.R.L.. It received FDA 510(k) clearance on 2007-11-26 under 510(k) number K072780. The device is classified under product code IZW. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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