LIFERAY FW MAMMO CASSETTE, LIFERAY KW MAMMO CASETTE— 510(k) K013229

Name: FDA 510(k) clearance K013229
Creator: U.S. Food and Drug Administration
Published: 2001-10-12

Substantially Equivalent

Ferrania USA, Inc.

FDA 510(k) clearance K013229 for LIFERAY FW MAMMO CASSETTE, LIFERAY KW MAMMO CASETTE, Substantially Equivalent on 2001-10-12. Applicant: Ferrania USA, Inc.. Device class: 2.

Clearance details

Applicant: Ferrania USA, Inc.
Product code: Code IXA
Device class: Class 2
Regulation: 21 CFR 892.1850
Advisory panel: Radiology
Date received: 2001-09-27
Decision date: 2001-10-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Weatherford, OK, US

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.