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FDA 510(k)

LIKEPAK 11 CARDIAC MONIT/LIFENET RS100 REC STATION

K-Number: K912189 · 1992-02-14

ApplicantPhysio-Control Corp.
Decision Date1992-02-14
Product CodeLOS
DecisionSubstantially Equivalent

Device Summary

LIKEPAK 11 CARDIAC MONIT/LIFENET RS100 REC STATION 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 1992-02-14 under 510(k) number K912189. The device is classified under product code LOS. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LIKEPAK 11 CARDIAC MONIT/LIFENET RS100 REC STATION?

LIKEPAK 11 CARDIAC MONIT/LIFENET RS100 REC STATION is a medical device that received FDA 510(k) clearance on 1992-02-14. The listed applicant is Physio-Control Corp.. The 510(k) number is K912189.

When did LIKEPAK 11 CARDIAC MONIT/LIFENET RS100 REC STATION receive FDA 510(k) clearance?

LIKEPAK 11 CARDIAC MONIT/LIFENET RS100 REC STATION received FDA 510(k) clearance on 1992-02-14, under 510(k) number K912189.

Who is the listed applicant for LIKEPAK 11 CARDIAC MONIT/LIFENET RS100 REC STATION?

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 LIKEPAK 11 CARDIAC MONIT/LIFENET RS100 REC STATION?

The FDA product code for LIKEPAK 11 CARDIAC MONIT/LIFENET RS100 REC STATION is LOS.

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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: LOS)

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.

K090895EKG-PLUS II SOFTWAREBionet Co., Ltd.K083749CARDIOVIEW32 REVIEW MODULEQrs Diagnostic, LLCK073376PHILIPS ECG ALGORITHMPhilips Medical SystemsK023034CARDIOTOUCH-3000Bionet Company, Ltd.K011328CARDIO CARE EKG-2000 12-CHANNEL ELECTROCARDIOGRAPHBionet Company, Ltd.K993616CARDIO-CARD INTERPRETATION SYSTEM INasiff Assoc., 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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