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WINNER SELF SEAL STERILIZATION POUCH

K051242 Class II Traditional
Decision Date
2005-12-13
Sponsor / Applicant
Winner Medical (Usa), Inc.

Technical Specification

510(k) Submission ID K051242
Product Code KCT
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.6850
Decision Date 2005-12-13
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

WINNER SELF SEAL STERILIZATION POUCH received FDA 510(k) clearance under submission number K051242, sponsored by Winner Medical (Usa), 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 2005-12-13.

Classification & Regulation

This clearance is catalogued under FDA product code KCT and 21 CFR 880.6850, within the General Hospital review panel as a Class II device.