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FDA 510(k)

ZOLL PD 2200 PACING-DEFIBRILLATION ELECTRODES

K-Number: K895032 · 1989-10-12

ApplicantZmi Corp.
Decision Date1989-10-12
Product CodeLDD
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

ZOLL PD 2200 PACING-DEFIBRILLATION ELECTRODES is the device name listed in this FDA 510(k) record. The listed applicant is Zmi Corp.. It received FDA 510(k) clearance on 1989-10-12 under 510(k) number K895032. 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 ZOLL PD 2200 PACING-DEFIBRILLATION ELECTRODES?

ZOLL PD 2200 PACING-DEFIBRILLATION ELECTRODES is a medical device that received FDA 510(k) clearance on 1989-10-12. The listed applicant is Zmi Corp.. The 510(k) number is K895032.

When did ZOLL PD 2200 PACING-DEFIBRILLATION ELECTRODES receive FDA 510(k) clearance?

ZOLL PD 2200 PACING-DEFIBRILLATION ELECTRODES received FDA 510(k) clearance on 1989-10-12, under 510(k) number K895032.

Who is the listed applicant for ZOLL PD 2200 PACING-DEFIBRILLATION ELECTRODES?

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

What is the FDA product code for ZOLL PD 2200 PACING-DEFIBRILLATION ELECTRODES?

The FDA product code for ZOLL PD 2200 PACING-DEFIBRILLATION ELECTRODES is LDD.

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Other records listing Zmi 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.

K915100BRINDLEY & SMITH ET-1000K915159PEDIATRIC MULTI-FUNCTION ELECTRODESK913484ZOLL D-900 DEFIBRILLATORK911956ZOLL PD-1400 PACER/DEFIBRILLATORK885166ZMI PART NO. NTP-2100, PEDIATRIC ELECTRODESK873402ZOLL NTP-1200 PACER/DEFIBRILLATOR

View all 8 devices →

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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