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FDA 510(k)

MODELS HP 43110MC, 43200MC W/CASE & 43200M NO CASE

K-Number: K893403 · 1989-08-03

ApplicantHewlett-Packard Co.
Decision Date1989-08-03
Product CodeLDD
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MODELS HP 43110MC, 43200MC W/CASE & 43200M NO CASE is the device name listed in this FDA 510(k) record. The listed applicant is Hewlett-Packard Co.. It received FDA 510(k) clearance on 1989-08-03 under 510(k) number K893403. 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 MODELS HP 43110MC, 43200MC W/CASE & 43200M NO CASE?

MODELS HP 43110MC, 43200MC W/CASE & 43200M NO CASE is a medical device that received FDA 510(k) clearance on 1989-08-03. The listed applicant is Hewlett-Packard Co.. The 510(k) number is K893403.

When did MODELS HP 43110MC, 43200MC W/CASE & 43200M NO CASE receive FDA 510(k) clearance?

MODELS HP 43110MC, 43200MC W/CASE & 43200M NO CASE received FDA 510(k) clearance on 1989-08-03, under 510(k) number K893403.

Who is the listed applicant for MODELS HP 43110MC, 43200MC W/CASE & 43200M NO CASE?

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

What is the FDA product code for MODELS HP 43110MC, 43200MC W/CASE & 43200M NO CASE?

The FDA product code for MODELS HP 43110MC, 43200MC W/CASE & 43200M NO CASE is LDD.

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Other records listing Hewlett-Packard Co. 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.

K992543HEARTSTREAM XLT DEFIBRILLATOR/MONITOR, AC CHARGER, DC CHARGER, DATA CARD, SINGLE BAY ADAPTER, DEFIBRILLATOR PADS CABLEK993587HP M2376A DEVICE LINK SYSTEMK993169MODIFICATION OF: PHYSIOLOGICAL SIGNAL TRANSMITTER AND RECEIVER, MODEL 3810AK992977HEWLETT PACKARD MULTIFUNCTION PEDIATRIC DEFIB FUNCTION, MODEL M3503A & M3504AK993516HP M2600A VIRIDIA TELEMETRY SYSTEMK993171HP VIRIDIA INFORMATION SYSTEM, MODELS M3150A/ M3151A/ M3153A/ M3154A

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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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