meddevicedb.com FDA Device Reference

DISPOSABLE STERILIZATION WRAP

K811242 Class II Traditional
Decision Date
1981-05-21
Sponsor / Applicant
Amsco Co.

Technical Specification

510(k) Submission ID K811242
Product Code FRG
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.6850
Decision Date 1981-05-21
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

DISPOSABLE STERILIZATION WRAP received FDA 510(k) clearance under submission number K811242, sponsored by Amsco Co.. 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 1981-05-21.

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.