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FDA 510(k)

LIFERAY FW MAMMO CASSETTE, LIFERAY KW MAMMO CASETTE

K-Number: K013229 · 2001-10-12

ApplicantFerrania USA, Inc.
Decision Date2001-10-12
Product CodeIXA
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

LIFERAY FW MAMMO CASSETTE, LIFERAY KW MAMMO CASETTE is the device name listed in this FDA 510(k) record. The listed applicant is Ferrania USA, Inc.. It received FDA 510(k) clearance on 2001-10-12 under 510(k) number K013229. The device is classified under product code IXA. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LIFERAY FW MAMMO CASSETTE, LIFERAY KW MAMMO CASETTE?

LIFERAY FW MAMMO CASSETTE, LIFERAY KW MAMMO CASETTE is a medical device that received FDA 510(k) clearance on 2001-10-12. The listed applicant is Ferrania USA, Inc.. The 510(k) number is K013229.

When did LIFERAY FW MAMMO CASSETTE, LIFERAY KW MAMMO CASETTE receive FDA 510(k) clearance?

LIFERAY FW MAMMO CASSETTE, LIFERAY KW MAMMO CASETTE received FDA 510(k) clearance on 2001-10-12, under 510(k) number K013229.

Who is the listed applicant for LIFERAY FW MAMMO CASSETTE, LIFERAY KW MAMMO CASETTE?

The FDA 510(k) record lists Ferrania USA, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LIFERAY FW MAMMO CASSETTE, LIFERAY KW MAMMO CASETTE?

The FDA product code for LIFERAY FW MAMMO CASSETTE, LIFERAY KW MAMMO CASETTE is IXA.

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Related Devices (Code: IXA)

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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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