MATRIX LR, LR 22A & LR/LASER RECORDER— 510(k) K860776

Name: FDA 510(k) clearance K860776
Creator: U.S. Food and Drug Administration
Published: 1986-06-16

Substantially Equivalent

Matrix Instruments

FDA 510(k) clearance K860776 for MATRIX LR, LR 22A & LR/LASER RECORDER, Substantially Equivalent on 1986-06-16. Applicant: Matrix Instruments. Device class: 2.

Clearance details

Applicant: Matrix Instruments
Product code: Code LMC
Device class: Class 2
Regulation: 21 CFR 892.2040
Advisory panel: Radiology
Date received: 1986-03-03
Decision date: 1986-06-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Orangeburg, NY, US

Download summary PDF View on FDA.gov ↗

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