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VITAL SIGNS MONITOR

K884938 Class II Traditional
Decision Date
1989-04-19
Sponsor / Applicant
Tico Medical Instruments, Inc.

Technical Specification

510(k) Submission ID K884938
Product Code DSK
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.1110
Decision Date 1989-04-19
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

VITAL SIGNS MONITOR received FDA 510(k) clearance under submission number K884938, sponsored by Tico Medical Instruments, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 1989-04-19.

Classification & Regulation

This clearance is catalogued under FDA product code DSK and 21 CFR 870.1110, within the Cardiovascular review panel as a Class II device.