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SMARTSPONGE SYSTEM

K071355 Class I Traditional
Decision Date
2007-05-24
Sponsor / Applicant
Clearcount Medical Solutions, Inc.

Technical Specification

510(k) Submission ID K071355
Product Code LWH
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.2740
Decision Date 2007-05-24
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SMARTSPONGE SYSTEM received FDA 510(k) clearance under submission number K071355, sponsored by Clearcount Medical Solutions, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the General Hospital review panel. The statutory decision date of record is 2007-05-24.

Classification & Regulation

This clearance is catalogued under FDA product code LWH and 21 CFR 880.2740, within the General Hospital review panel as a Class I device.