MATRIX LD & LD/LASER DIGITIZER— 510(k) K860777

Name: FDA 510(k) clearance K860777
Creator: U.S. Food and Drug Administration
Published: 1987-04-22

Substantially Equivalent

Matrix Instruments

FDA 510(k) clearance K860777 for MATRIX LD & LD/LASER DIGITIZER, Substantially Equivalent on 1987-04-22. Applicant: Matrix Instruments. Device class: 2.

Clearance details

Applicant: Matrix Instruments
Product code: Code LMA
Device class: Class 2
Regulation: 21 CFR 892.2030
Advisory panel: Radiology
Date received: 1986-03-03
Decision date: 1987-04-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Orangeburg, NY, US

Download summary PDF View on FDA.gov ↗

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