meddevicedb.com FDA Device Reference

STERILE DRESSING PACK

K800490 Class II Traditional
Decision Date
1980-03-12
Sponsor / Applicant
Medi-Spec

Technical Specification

510(k) Submission ID K800490
Product Code KKX
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4370
Decision Date 1980-03-12
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

STERILE DRESSING PACK received FDA 510(k) clearance under submission number K800490, sponsored by Medi-Spec. The device was reviewed via the Traditional premarket notification pathway and assigned to the General, Plastic Surgery review panel. The statutory decision date of record is 1980-03-12.

Classification & Regulation

This clearance is catalogued under FDA product code KKX and 21 CFR 878.4370, within the General, Plastic Surgery review panel as a Class II device.