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FDA 510(k)

MATRX DISPOSABLE NON-INVASIVE GELLED PACING ELEC.

K-Number: K900551 · 1990-05-09

ApplicantMatrix Medica, Inc.
Decision Date1990-05-09
Product CodeDRS
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MATRX DISPOSABLE NON-INVASIVE GELLED PACING ELEC. is the device name listed in this FDA 510(k) record. The listed applicant is Matrix Medica, Inc.. It received FDA 510(k) clearance on 1990-05-09 under 510(k) number K900551. The device is classified under product code DRS. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MATRX DISPOSABLE NON-INVASIVE GELLED PACING ELEC.?

MATRX DISPOSABLE NON-INVASIVE GELLED PACING ELEC. is a medical device that received FDA 510(k) clearance on 1990-05-09. The listed applicant is Matrix Medica, Inc.. The 510(k) number is K900551.

When did MATRX DISPOSABLE NON-INVASIVE GELLED PACING ELEC. receive FDA 510(k) clearance?

MATRX DISPOSABLE NON-INVASIVE GELLED PACING ELEC. received FDA 510(k) clearance on 1990-05-09, under 510(k) number K900551.

Who is the listed applicant for MATRX DISPOSABLE NON-INVASIVE GELLED PACING ELEC.?

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

What is the FDA product code for MATRX DISPOSABLE NON-INVASIVE GELLED PACING ELEC.?

The FDA product code for MATRX DISPOSABLE NON-INVASIVE GELLED PACING ELEC. is DRS.

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Related Devices (Code: DRS)

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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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