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EXTERNAL PACEMAKER ANALYZER, MODEL PMT 100

K961582 Class II Traditional
Decision Date
1996-11-08
Sponsor / Applicant
North American Technical Services Corp.

Technical Specification

510(k) Submission ID K961582
Product Code DTC
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.3630
Decision Date 1996-11-08
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

EXTERNAL PACEMAKER ANALYZER, MODEL PMT 100 received FDA 510(k) clearance under submission number K961582, sponsored by North American Technical Services 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 1996-11-08.

Classification & Regulation

This clearance is catalogued under FDA product code DTC and 21 CFR 870.3630, within the Cardiovascular review panel as a Class II device.