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FDA 510(k)

MDPHONE CELLULAR + RESCUE (DEFIB SYSTEM)

K-Number: K911604 · 1991-09-23

ApplicantMedphone Corp.
Decision Date1991-09-23
Product CodeLDD
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MDPHONE CELLULAR + RESCUE (DEFIB SYSTEM) is the device name listed in this FDA 510(k) record. The listed applicant is Medphone Corp.. It received FDA 510(k) clearance on 1991-09-23 under 510(k) number K911604. 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 MDPHONE CELLULAR + RESCUE (DEFIB SYSTEM)?

MDPHONE CELLULAR + RESCUE (DEFIB SYSTEM) is a medical device that received FDA 510(k) clearance on 1991-09-23. The listed applicant is Medphone Corp.. The 510(k) number is K911604.

When did MDPHONE CELLULAR + RESCUE (DEFIB SYSTEM) receive FDA 510(k) clearance?

MDPHONE CELLULAR + RESCUE (DEFIB SYSTEM) received FDA 510(k) clearance on 1991-09-23, under 510(k) number K911604.

Who is the listed applicant for MDPHONE CELLULAR + RESCUE (DEFIB SYSTEM)?

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

What is the FDA product code for MDPHONE CELLULAR + RESCUE (DEFIB SYSTEM)?

The FDA product code for MDPHONE CELLULAR + RESCUE (DEFIB SYSTEM) is LDD.

Related Clinical Trials

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.

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Other records listing Medphone 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.

K864257TELEPHONE DEFIBRILLATOR SYSTEM

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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