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FDA 510(k)

DEFIB-PADS

K-Number: K855082 · 1986-03-31

ApplicantConmedcorp
Decision Date1986-03-31
Product CodeLDD
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

DEFIB-PADS is the device name listed in this FDA 510(k) record. The listed applicant is Conmedcorp. It received FDA 510(k) clearance on 1986-03-31 under 510(k) number K855082. 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 DEFIB-PADS?

DEFIB-PADS is a medical device that received FDA 510(k) clearance on 1986-03-31. The listed applicant is Conmedcorp. The 510(k) number is K855082.

When did DEFIB-PADS receive FDA 510(k) clearance?

DEFIB-PADS received FDA 510(k) clearance on 1986-03-31, under 510(k) number K855082.

Who is the listed applicant for DEFIB-PADS?

The FDA 510(k) record lists Conmedcorp as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DEFIB-PADS?

The FDA product code for DEFIB-PADS is LDD.

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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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