meddevicedb.com FDA Device Reference

Medicom Sterilization Wrap

K240862 Class II Traditional
Decision Date
2024-06-21
Sponsor / Applicant
Medicom Group, Inc.

Technical Specification

510(k) Submission ID K240862
Product Code FRG
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.6850
Decision Date 2024-06-21
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Medicom Sterilization Wrap received FDA 510(k) clearance under submission number K240862, sponsored by Medicom Group, 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 2024-06-21.

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.