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URESIL ABSCESS DRIANAGE AND IRRIGATION SET

K925117 Class I Traditional
Decision Date
1993-08-11
Sponsor / Applicant
Uresil Corp.

Technical Specification

510(k) Submission ID K925117
Product Code GBX
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4200
Decision Date 1993-08-11
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

URESIL ABSCESS DRIANAGE AND IRRIGATION SET received FDA 510(k) clearance under submission number K925117, sponsored by Uresil Corp.. 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 1993-08-11.

Classification & Regulation

This clearance is catalogued under FDA product code GBX and 21 CFR 878.4200, within the General, Plastic Surgery review panel as a Class I device.