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FDA 510(k)

GRI LASERGRAPH(TM) ECG PAPER

K-Number: K902586 · 1990-06-22

Decision Date1990-06-22
Product CodeDSF
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

GRI LASERGRAPH(TM) ECG PAPER is the device name listed in this FDA 510(k) record. The listed applicant is Gri Medical Products, Inc.. It received FDA 510(k) clearance on 1990-06-22 under 510(k) number K902586. The device is classified under product code DSF. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GRI LASERGRAPH(TM) ECG PAPER?

GRI LASERGRAPH(TM) ECG PAPER is a medical device that received FDA 510(k) clearance on 1990-06-22. The listed applicant is Gri Medical Products, Inc.. The 510(k) number is K902586.

When did GRI LASERGRAPH(TM) ECG PAPER receive FDA 510(k) clearance?

GRI LASERGRAPH(TM) ECG PAPER received FDA 510(k) clearance on 1990-06-22, under 510(k) number K902586.

Who is the listed applicant for GRI LASERGRAPH(TM) ECG PAPER?

The FDA 510(k) record lists Gri Medical Products, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for GRI LASERGRAPH(TM) ECG PAPER?

The FDA product code for GRI LASERGRAPH(TM) ECG PAPER is DSF.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Related Devices (Code: DSF)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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