GRI LASERGRAPH(TM) ECG PAPER— 510(k) K902586

Name: FDA 510(k) clearance K902586
Creator: U.S. Food and Drug Administration
Published: 1990-06-22

Substantially Equivalent

Gri Medical Products, Inc.

FDA 510(k) clearance K902586 for GRI LASERGRAPH(TM) ECG PAPER, Substantially Equivalent on 1990-06-22. Applicant: Gri Medical Products, Inc.. Device class: 1.

Clearance details

Applicant: Gri Medical Products, Inc.
Product code: Code DSF
Device class: Class 1
Regulation: 21 CFR 870.2810
Advisory panel: Cardiovascular
Date received: 1990-06-12
Decision date: 1990-06-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Norwalk, CT, US

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