meddevicedb.com FDA Device Reference

TYVEK SELF-SEAL POUCHES ,TYVEK HEAT-SEAL ROLLS

K112087 Class II Traditional
Decision Date
2012-10-15
Sponsor / Applicant
Advanced Sterilization Products

Technical Specification

510(k) Submission ID K112087
Product Code KCT
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.6850
Decision Date 2012-10-15
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

TYVEK SELF-SEAL POUCHES ,TYVEK HEAT-SEAL ROLLS received FDA 510(k) clearance under submission number K112087, sponsored by Advanced Sterilization Products. 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 2012-10-15.

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.