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HOLTER PERFORMER FEATHER WEIGHT/CASS

K833823 Class II Traditional
Decision Date
1983-12-01
Sponsor / Applicant
Applied Cardiac Systems

Technical Specification

510(k) Submission ID K833823
Product Code DSH
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.2800
Decision Date 1983-12-01
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

HOLTER PERFORMER FEATHER WEIGHT/CASS received FDA 510(k) clearance under submission number K833823, sponsored by Applied Cardiac Systems. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 1983-12-01.

Classification & Regulation

This clearance is catalogued under FDA product code DSH and 21 CFR 870.2800, within the Cardiovascular review panel as a Class II device.