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SURVIVALINK MULTIFUNCTIONAL ELECTRODE (SVL-9630)

K993072 Class III Traditional
Decision Date
1999-12-10
Sponsor / Applicant
Survivalink Corp.

Technical Specification

510(k) Submission ID K993072
Product Code MKJ
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.5310
Decision Date 1999-12-10
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SURVIVALINK MULTIFUNCTIONAL ELECTRODE (SVL-9630) received FDA 510(k) clearance under submission number K993072, sponsored by Survivalink Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 1999-12-10.

Classification & Regulation

This clearance is catalogued under FDA product code MKJ and 21 CFR 870.5310, within the Cardiovascular review panel as a Class III device.