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FDA 510(k)

ZOLL NTP-1200 PACER/DEFIBRILLATOR

K-Number: K873402 · 1987-11-23

ApplicantZmi Corp.
Decision Date1987-11-23
Product CodeDRO
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

ZOLL NTP-1200 PACER/DEFIBRILLATOR is the device name listed in this FDA 510(k) record. The listed applicant is Zmi Corp.. It received FDA 510(k) clearance on 1987-11-23 under 510(k) number K873402. The device is classified under product code DRO. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ZOLL NTP-1200 PACER/DEFIBRILLATOR?

ZOLL NTP-1200 PACER/DEFIBRILLATOR is a medical device that received FDA 510(k) clearance on 1987-11-23. The listed applicant is Zmi Corp.. The 510(k) number is K873402.

When did ZOLL NTP-1200 PACER/DEFIBRILLATOR receive FDA 510(k) clearance?

ZOLL NTP-1200 PACER/DEFIBRILLATOR received FDA 510(k) clearance on 1987-11-23, under 510(k) number K873402.

Who is the listed applicant for ZOLL NTP-1200 PACER/DEFIBRILLATOR?

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 NTP-1200 PACER/DEFIBRILLATOR?

The FDA product code for ZOLL NTP-1200 PACER/DEFIBRILLATOR is DRO.

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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/DEFIBRILLATORK895032ZOLL PD 2200 PACING-DEFIBRILLATION ELECTRODESK885166ZMI PART NO. NTP-2100, PEDIATRIC ELECTRODES

View all 8 devices →

Related Devices (Code: DRO)

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.

K012218LUDLOW GRADIENT EDGE ADULT & PEDIATRIC MULTIFUNCTIONAL ELECTRODESThe Ludlow Company LPK012404K-DEFIB/PACE ADULT ELECTRODE, MODEL KDP-85Katecho, Inc.K000660ESCORT II+ 400 SERIES (ESCORT PRISM), MODEL 20400, 20401, 20403, MONITOR, MODELS 20411, 20412, 20413Medical Data ElectronicsK983196PADTAK PACE/DEFIB/CARDIOVERT MONITORING ELECTRODE(S)Tz Medical, Inc.K983232PADTAK PEDIATRIC DEFIB/CARDIOVERT/PACE/MONITOR-RADIOTRANSPARENT (2X2.25),MODEL 2602, PADTAK PEDIATRIC DEFIB/CARDIOVERTTz Medical, Inc.K974034PORTABLE INTENSIVE CARE UNITMedical Research Laboratories, 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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