LIFERAY WL CASSETTE, LIFERAY KW CASSETTE
K-Number: K012373 · 2001-08-09
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Device Summary
Frequently Asked Questions
What is the LIFERAY WL CASSETTE, LIFERAY KW CASSETTE?
LIFERAY WL CASSETTE, LIFERAY KW CASSETTE is a medical device that received FDA 510(k) clearance on 2001-08-09. The listed applicant is Ferrania S.P.A.. The 510(k) number is K012373.
When did LIFERAY WL CASSETTE, LIFERAY KW CASSETTE receive FDA 510(k) clearance?
LIFERAY WL CASSETTE, LIFERAY KW CASSETTE received FDA 510(k) clearance on 2001-08-09, under 510(k) number K012373.
Who is the listed applicant for LIFERAY WL CASSETTE, LIFERAY KW CASSETTE?
The FDA 510(k) record lists Ferrania S.P.A. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for LIFERAY WL CASSETTE, LIFERAY KW CASSETTE?
The FDA product code for LIFERAY WL CASSETTE, LIFERAY KW CASSETTE is IXA.
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 Ferrania S.P.A. 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: IXA)
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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