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FDA 510(k)

LIFEPAK 5 CARDIOSCOPE-RECORDER MODULE

K-Number: K760676 · 1976-10-13

ApplicantPhysio-Control Corp.
Decision Date1976-10-13
Product CodeDSF
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

LIFEPAK 5 CARDIOSCOPE-RECORDER MODULE 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 1976-10-13 under 510(k) number K760676. 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 LIFEPAK 5 CARDIOSCOPE-RECORDER MODULE?

LIFEPAK 5 CARDIOSCOPE-RECORDER MODULE is a medical device that received FDA 510(k) clearance on 1976-10-13. The listed applicant is Physio-Control Corp.. The 510(k) number is K760676.

When did LIFEPAK 5 CARDIOSCOPE-RECORDER MODULE receive FDA 510(k) clearance?

LIFEPAK 5 CARDIOSCOPE-RECORDER MODULE received FDA 510(k) clearance on 1976-10-13, under 510(k) number K760676.

Who is the listed applicant for LIFEPAK 5 CARDIOSCOPE-RECORDER MODULE?

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 LIFEPAK 5 CARDIOSCOPE-RECORDER MODULE?

The FDA product code for LIFEPAK 5 CARDIOSCOPE-RECORDER MODULE is DSF.

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Other records listing Physio-Control Corp. 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.

K991910LIFEPAK 12 BIPHASICK990338NIBP AND CO2 OPTIONS FOR THE PHYSIO-CONTROL LIFEPAK 12 DEFIBRILLATOR/MONITOR SYSTEMK983393LIFEPAK 500 BIPHASICK973486LIFE PAK 12K962359LIFEPAK 300K955854LIFEPAK 500

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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.

K910871EDENTEC DIGITAL CHARTER MODEL 3710Edentec Corp.K912929DASH IVAstro-Med, Inc.K905856MODEL 556 MONITORGe Medical Systems Information TechnologiesK902586GRI LASERGRAPH(TM) ECG PAPERGri Medical Products, Inc.K902230COLORADO COLOR IMAGING RECORDERHoneywell, Inc.K901385GABRIEL MEDICAL CLS THERMAL RECORDERGabriel Medical, 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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