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FDA 510(k)

LIMB LEAD SEL. (ECG LEAD SWITCHING AD.)

K-Number: K761210 · 1976-12-21

ApplicantPhysio-Control Corp.
Decision Date1976-12-21
Product CodeDRW
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

LIMB LEAD SEL. (ECG LEAD SWITCHING AD.) 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 1976-12-21 under 510(k) number K761210. The device is classified under product code DRW. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LIMB LEAD SEL. (ECG LEAD SWITCHING AD.)?

LIMB LEAD SEL. (ECG LEAD SWITCHING AD.) is a medical device that received FDA 510(k) clearance on 1976-12-21. The listed applicant is Physio-Control Corp.. The 510(k) number is K761210.

When did LIMB LEAD SEL. (ECG LEAD SWITCHING AD.) receive FDA 510(k) clearance?

LIMB LEAD SEL. (ECG LEAD SWITCHING AD.) received FDA 510(k) clearance on 1976-12-21, under 510(k) number K761210.

Who is the listed applicant for LIMB LEAD SEL. (ECG LEAD SWITCHING AD.)?

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 LIMB LEAD SEL. (ECG LEAD SWITCHING AD.)?

The FDA product code for LIMB LEAD SEL. (ECG LEAD SWITCHING AD.) is DRW.

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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: DRW)

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.

K033513EASI ECG ALGORITHMPhilips Medical SystemsK020456EASI 12 LEAD ALGORITHMPhilips Medical SystemsK930786EPCORSiemens Medical Solutions USA, Inc.K872781EASI LEAD SYSTEM CABLE ASSEMBLYTotemite Medical ElectronicsK861981ELECTROCARDIOGRAPH LEAD SWITCHING ADAPTORVital Signs, Inc.K851627KBX-20 OUTBOARD KEYBOARD ACCESS. FOR G-2000 ELECTREaton Medical Group

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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