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REAVILLMED PRESSURE MONITORING SYSTEM AND PICC

K101189 Class II Traditional
Decision Date
2010-12-22
Sponsor / Applicant
Reavillmed

Technical Specification

510(k) Submission ID K101189
Product Code DRS
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.2850
Decision Date 2010-12-22
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

REAVILLMED PRESSURE MONITORING SYSTEM AND PICC received FDA 510(k) clearance under submission number K101189, sponsored by Reavillmed. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2010-12-22.

Classification & Regulation

This clearance is catalogued under FDA product code DRS and 21 CFR 870.2850, within the Cardiovascular review panel as a Class II device.