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MODEL 263 SPECTRASCAN(TM) HOLTER ANALYSIS SYSTEM

K896862 Class II Traditional
Decision Date
1990-04-18
Sponsor / Applicant
Del Mar Avionics

Technical Specification

510(k) Submission ID K896862
Product Code DSI
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.1025
Decision Date 1990-04-18
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MODEL 263 SPECTRASCAN(TM) HOLTER ANALYSIS SYSTEM received FDA 510(k) clearance under submission number K896862, sponsored by Del Mar Avionics. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 1990-04-18.

Classification & Regulation

This clearance is catalogued under FDA product code DSI and 21 CFR 870.1025, within the Cardiovascular review panel as a Class II device.