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FDA 510(k)

450SLL DEFIBRILLATOR

K-Number: K874204 · 1988-01-28

ApplicantMedical Research Laboratories, Inc.
Decision Date1988-01-28
Product CodeLDD
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

450SLL DEFIBRILLATOR is the device name listed in this FDA 510(k) record. The listed applicant is Medical Research Laboratories, Inc.. It received FDA 510(k) clearance on 1988-01-28 under 510(k) number K874204. The device is classified under product code LDD. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the 450SLL DEFIBRILLATOR?

450SLL DEFIBRILLATOR is a medical device that received FDA 510(k) clearance on 1988-01-28. The listed applicant is Medical Research Laboratories, Inc.. The 510(k) number is K874204.

When did 450SLL DEFIBRILLATOR receive FDA 510(k) clearance?

450SLL DEFIBRILLATOR received FDA 510(k) clearance on 1988-01-28, under 510(k) number K874204.

Who is the listed applicant for 450SLL DEFIBRILLATOR?

The FDA 510(k) record lists Medical Research Laboratories, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for 450SLL DEFIBRILLATOR?

The FDA product code for 450SLL DEFIBRILLATOR is LDD.

Related Clinical Trials

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Other records listing Medical Research Laboratories, Inc. 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.

K021168JUMP START, MODEL 970300K012766PORTABLE INTENSIVE CARE UNITK012030PORTABLE INTENSIVE CARE UNITK010207PORTABLE INSTENSIVE CARE UNITK002232AEDEFIBRILLATORK000712PORTABLE INTENSIVE CARE UNIT, MODEL PIC

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Related Devices (Code: LDD)

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.

K203231Switched Internal PaddlesPhilips North America, LLCK200849Tempus LS - ManualRemote Diagnostic Technologies, Ltd. A Philips CompanyK182503Sterilizable Internal Defibrillation Paddles for use with LIFEPAK defibrillators/monitorsPhysio-Control, Inc.K103651CARDIOMEDCardio Medical Products, Inc.K103783EURO DEFI PADS ADULT; EURO DEFI PADS ADULT RADIOTRANSPARENT: EURO DEFI PADS PEDIATRICFiab SpaK103334CARDIO MEDCardio Medical Products, 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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