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TCPM II TOURNIQUET CUFF PRESSURE MONITOR

K900104 Class I Traditional
Decision Date
1990-03-15
Sponsor / Applicant
Electromedics, Inc.

Technical Specification

510(k) Submission ID K900104
Product Code KCY
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.5910
Decision Date 1990-03-15
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

TCPM II TOURNIQUET CUFF PRESSURE MONITOR received FDA 510(k) clearance under submission number K900104, sponsored by Electromedics, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the General, Plastic Surgery review panel. The statutory decision date of record is 1990-03-15.

Classification & Regulation

This clearance is catalogued under FDA product code KCY and 21 CFR 878.5910, within the General, Plastic Surgery review panel as a Class I device.