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FDA 510(k)

K-DEFIB/PACE CARBON ELECTRODE

K-Number: K926175 · 1993-04-15

ApplicantKatecho, Inc.
Decision Date1993-04-15
Product CodeDRO
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

K-DEFIB/PACE CARBON ELECTRODE is the device name listed in this FDA 510(k) record. The listed applicant is Katecho, Inc.. It received FDA 510(k) clearance on 1993-04-15 under 510(k) number K926175. 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 K-DEFIB/PACE CARBON ELECTRODE?

K-DEFIB/PACE CARBON ELECTRODE is a medical device that received FDA 510(k) clearance on 1993-04-15. The listed applicant is Katecho, Inc.. The 510(k) number is K926175.

When did K-DEFIB/PACE CARBON ELECTRODE receive FDA 510(k) clearance?

K-DEFIB/PACE CARBON ELECTRODE received FDA 510(k) clearance on 1993-04-15, under 510(k) number K926175.

Who is the listed applicant for K-DEFIB/PACE CARBON ELECTRODE?

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

What is the FDA product code for K-DEFIB/PACE CARBON ELECTRODE?

The FDA product code for K-DEFIB/PACE CARBON ELECTRODE is DRO.

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Other records listing Katecho, Inc. 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.

K012404K-DEFIB/PACE ADULT ELECTRODE, MODEL KDP-85K010543KM-30 TENS ELECTRODEK003228K-DEFIB/PACE MULTIFUCTION PEDIATRIC ELECTRODE, MODEL KDP-70AK002806K-DEFIB/PACE, MODEL KDP-60AK000870KM-10 TENS ELECTRODEK993745K-DEFIB/PACE ADULT ELECTRODE, MODEL KDP-80

View all 26 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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