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ZOLL AUTOCLAVABLE INTERNAL HANDLES, ZOLL AUTOCLAVABLE INTERNAL HANDLES WITH INTEGRATED ELECTRODES, ZOLL AUTOCLAVABLE

K042302 Class II Special
Decision Date
2004-10-26
Sponsor / Applicant
Zoll Medical Corp

Technical Specification

510(k) Submission ID K042302
Product Code LDD
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.5300
Decision Date 2004-10-26
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ZOLL AUTOCLAVABLE INTERNAL HANDLES, ZOLL AUTOCLAVABLE INTERNAL HANDLES WITH INTEGRATED ELECTRODES, ZOLL AUTOCLAVABLE received FDA 510(k) clearance under submission number K042302, sponsored by Zoll Medical Corp. The device was reviewed via the Special premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2004-10-26.

Classification & Regulation

This clearance is catalogued under FDA product code LDD and 21 CFR 870.5300, within the Cardiovascular review panel as a Class II device.