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DATAMEDIX PECGASYS SYSTEM

K810027 Class II Traditional
Decision Date
1981-03-26
Sponsor / Applicant
Datamedix

Technical Specification

510(k) Submission ID K810027
Product Code DSI
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.1025
Decision Date 1981-03-26
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

DATAMEDIX PECGASYS SYSTEM received FDA 510(k) clearance under submission number K810027, sponsored by Datamedix. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 1981-03-26.

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.