FDA 510(k)

R 72

K-Number: K030487 · 2003-08-01

Decision Date2003-08-01

Product CodeKPW

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

R 72 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 2003-08-01 under 510(k) number K030487. The device is classified under product code KPW. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the R 72?

R 72 is a medical device that received FDA 510(k) clearance on 2003-08-01. The listed applicant is Ralco S.R.L.. The 510(k) number is K030487.

When did R 72 receive FDA 510(k) clearance?

R 72 received FDA 510(k) clearance on 2003-08-01, under 510(k) number K030487.

Who is the listed applicant for R 72?

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 R 72?

The FDA product code for R 72 is KPW.

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.

K110856RALCO K091517RALCO, MODEL R225 ACS K083029MODEL R605DASM AUTOMATIC X-RAY COLLIMATOR K072780MODEL R302DACS/A AUTOMATIC X-RAY COLLIMATOR K946320R 302

Related Devices (Code: KPW)

K093596LUMOS, MODEL R 72BLumos, Inc.K062788COLLIMATOR, MODEL M-38Umi International K954310BLA-800AToshiba Medical Systems K946320R 302Ralco S.R.L.K914184P2020-8-0 BEAM-LIMITING DEVICEPrecise Optics K904587DENSICOMP 250L. Keroack Co.

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.