FDA 510(k)

DEFIBRILLATOR INTERAL PADDLE TEST LOAD

K-Number: K790394 · 1979-03-23

Decision Date1979-03-23

Product CodeDRL

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

DEFIBRILLATOR INTERAL PADDLE TEST LOAD is the device name listed in this FDA 510(k) record. The listed applicant is Physio-Control Corp.. It received FDA 510(k) clearance on 1979-03-23 under 510(k) number K790394. 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 DEFIBRILLATOR INTERAL PADDLE TEST LOAD?

DEFIBRILLATOR INTERAL PADDLE TEST LOAD is a medical device that received FDA 510(k) clearance on 1979-03-23. The listed applicant is Physio-Control Corp.. The 510(k) number is K790394.

When did DEFIBRILLATOR INTERAL PADDLE TEST LOAD receive FDA 510(k) clearance?

DEFIBRILLATOR INTERAL PADDLE TEST LOAD received FDA 510(k) clearance on 1979-03-23, under 510(k) number K790394.

Who is the listed applicant for DEFIBRILLATOR INTERAL PADDLE TEST LOAD?

The FDA 510(k) record lists Physio-Control Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DEFIBRILLATOR INTERAL PADDLE TEST LOAD?

The FDA product code for DEFIBRILLATOR INTERAL PADDLE TEST LOAD is DRL.

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Other records listing Physio-Control Corp. as applicant

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Related Devices (Code: DRL)

K190437Delta 3300Netech Corporation K182905UniPulseSeaward Group K110192DEFIBRILLATOR ANALYZER - DA-2006PBc Group International, Inc.K083347IMPULSE 7010 DEFIBRILLATOR SELECTABLE LOADSFluke Biomedical K072114IMPULSE 6000D/7000DPFluke Biomedical K062099PHASE 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.