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FDA 510(k)

MATRX BATTERY CHARGER/DEFIBRILLATOR TESTER

K-Number: K895525 · 1990-01-26

ApplicantMatrix Medica, Inc.
Decision Date1990-01-26
Product CodeDRL
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MATRX BATTERY CHARGER/DEFIBRILLATOR TESTER 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 1990-01-26 under 510(k) number K895525. The device is classified under product code DRL. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MATRX BATTERY CHARGER/DEFIBRILLATOR TESTER?

MATRX BATTERY CHARGER/DEFIBRILLATOR TESTER is a medical device that received FDA 510(k) clearance on 1990-01-26. The listed applicant is Matrix Medica, Inc.. The 510(k) number is K895525.

When did MATRX BATTERY CHARGER/DEFIBRILLATOR TESTER receive FDA 510(k) clearance?

MATRX BATTERY CHARGER/DEFIBRILLATOR TESTER received FDA 510(k) clearance on 1990-01-26, under 510(k) number K895525.

Who is the listed applicant for MATRX BATTERY CHARGER/DEFIBRILLATOR TESTER?

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 BATTERY CHARGER/DEFIBRILLATOR TESTER?

The FDA product code for MATRX BATTERY CHARGER/DEFIBRILLATOR TESTER is DRL.

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.

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Other records listing Matrix Medica, Inc. as applicant

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.

K961536FLEXSCOPEK923693KLORMANK921982MATRX HOPE(R) 5 RESUSCITATORK915353MATRX MEDICAL MAXIMIZER 1000 AND 2000 VACUUM PUMPK912661MATRX, PYRAMID TRIANGLE BANDAGEK900551MATRX DISPOSABLE NON-INVASIVE GELLED PACING ELEC.

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Related Devices (Code: DRL)

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.

K190437Delta 3300Netech CorporationK182905UniPulseSeaward GroupK110192DEFIBRILLATOR ANALYZER - DA-2006PBc Group International, Inc.K083347IMPULSE 7010 DEFIBRILLATOR SELECTABLE LOADSFluke BiomedicalK072114IMPULSE 6000D/7000DPFluke BiomedicalK062099PHASE 3, MODEL DT-1Datrend Systems, Inc.

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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