FILM PROCESSOR, MODEL LIFE RAY PRO 1000— 510(k) K023801

Name: FDA 510(k) clearance K023801
Creator: U.S. Food and Drug Administration
Published: 2003-02-12

Substantially Equivalent

S.A.I.E.P. S.R.L.

FDA 510(k) clearance K023801 for FILM PROCESSOR, MODEL LIFE RAY PRO 1000, Substantially Equivalent on 2003-02-12. Applicant: S.A.I.E.P. S.R.L.. Device class: 2.

Clearance details

Applicant: S.A.I.E.P. S.R.L.
Product code: Code IXW
Device class: Class 2
Regulation: 21 CFR 892.1900
Advisory panel: Radiology
Date received: 2002-11-14
Decision date: 2003-02-12
Decision: Substantially Equivalent
Clearance type: Abbreviated
Location: Weatherford, OK, US

Download summary PDF View on FDA.gov ↗

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