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PMSSteripack Self-Seal Sterilization Pouch with Chemical Indicator (KP)

K152669 Class II Traditional
Decision Date
2016-01-15
Sponsor / Applicant
Pms Tip Teknolojileri Sanayi VE Ticaret Limited Std

Technical Specification

510(k) Submission ID K152669
Product Code FRG
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.6850
Decision Date 2016-01-15
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PMSSteripack Self-Seal Sterilization Pouch with Chemical Indicator (KP) received FDA 510(k) clearance under submission number K152669, sponsored by Pms Tip Teknolojileri Sanayi VE Ticaret Limited Std. 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 2016-01-15.

Classification & Regulation

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