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FDA 510(k)

LIFEPAK 7 ACUTE CARDIAC CARE SYSTEM

K-Number: K810154 · 1981-03-26

ApplicantPhysio-Control Corp.
Decision Date1981-03-26
Product CodeDPS
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

LIFEPAK 7 ACUTE CARDIAC CARE SYSTEM 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 1981-03-26 under 510(k) number K810154. The device is classified under product code DPS. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LIFEPAK 7 ACUTE CARDIAC CARE SYSTEM?

LIFEPAK 7 ACUTE CARDIAC CARE SYSTEM is a medical device that received FDA 510(k) clearance on 1981-03-26. The listed applicant is Physio-Control Corp.. The 510(k) number is K810154.

When did LIFEPAK 7 ACUTE CARDIAC CARE SYSTEM receive FDA 510(k) clearance?

LIFEPAK 7 ACUTE CARDIAC CARE SYSTEM received FDA 510(k) clearance on 1981-03-26, under 510(k) number K810154.

Who is the listed applicant for LIFEPAK 7 ACUTE CARDIAC CARE SYSTEM?

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 7 ACUTE CARDIAC CARE SYSTEM?

The FDA product code for LIFEPAK 7 ACUTE CARDIAC CARE SYSTEM is DPS.

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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: DPS)

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.

K254255S-Patch CardioAIWellysis Corp.K252463SE-1202 Series Electrocardiograph (Model: SE-1202, SE-1202E)Edan Instruments, Inc.K251670MAC 7 Resting ECG Analysis SystemGe Medical Systems Information Technologies, Inc.K252361AccurECG Analysis System (v2.0)Accurkardia, Inc.K252474Withings BeamO (SCT02)WithingsK250569Cardiologs Holter PlatformPhilips France Commercial

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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