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SURGICOUNT SAFETY-SPONGE SYSTEM

K060076 Class I Traditional
Decision Date
2006-03-14
Sponsor / Applicant
Surgicount Medical

Technical Specification

510(k) Submission ID K060076
Product Code LWH
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.2740
Decision Date 2006-03-14
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SURGICOUNT SAFETY-SPONGE SYSTEM received FDA 510(k) clearance under submission number K060076, sponsored by Surgicount Medical. 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 2006-03-14.

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.