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FDA 510(k)

CARDIOTEST EK 53 R, CARDIOGNOST EK 56/ EK 512

K-Number: K900246 · 1990-07-03

ApplicantPpg Industries, Inc.
Decision Date1990-07-03
Product CodeDSI
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

CARDIOTEST EK 53 R, CARDIOGNOST EK 56/ EK 512 is the device name listed in this FDA 510(k) record. The listed applicant is Ppg Industries, Inc.. It received FDA 510(k) clearance on 1990-07-03 under 510(k) number K900246. The device is classified under product code DSI. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CARDIOTEST EK 53 R, CARDIOGNOST EK 56/ EK 512?

CARDIOTEST EK 53 R, CARDIOGNOST EK 56/ EK 512 is a medical device that received FDA 510(k) clearance on 1990-07-03. The listed applicant is Ppg Industries, Inc.. The 510(k) number is K900246.

When did CARDIOTEST EK 53 R, CARDIOGNOST EK 56/ EK 512 receive FDA 510(k) clearance?

CARDIOTEST EK 53 R, CARDIOGNOST EK 56/ EK 512 received FDA 510(k) clearance on 1990-07-03, under 510(k) number K900246.

Who is the listed applicant for CARDIOTEST EK 53 R, CARDIOGNOST EK 56/ EK 512?

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

What is the FDA product code for CARDIOTEST EK 53 R, CARDIOGNOST EK 56/ EK 512?

The FDA product code for CARDIOTEST EK 53 R, CARDIOGNOST EK 56/ EK 512 is DSI.

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Official Source

View on FDA Database →

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

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