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ELCAT D-PPG, PLETHYSMOGRAPH DEVICE

K944395 Class II Traditional
Decision Date
1995-05-10
Sponsor / Applicant
Dermatology Assoc.

Technical Specification

510(k) Submission ID K944395
Product Code JOM
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.2780
Decision Date 1995-05-10
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ELCAT D-PPG, PLETHYSMOGRAPH DEVICE received FDA 510(k) clearance under submission number K944395, sponsored by Dermatology Assoc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 1995-05-10.

Classification & Regulation

This clearance is catalogued under FDA product code JOM and 21 CFR 870.2780, within the Cardiovascular review panel as a Class II device.