meddevicedb.com FDA Device Reference

WELLS LAMONT HANDAGES/MED WRAP DRESSINGS

K925937 Class I Traditional
Decision Date
1993-08-09
Sponsor / Applicant
Wells Lamont Corp.

Technical Specification

510(k) Submission ID K925937
Product Code KMF
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5090
Decision Date 1993-08-09
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

WELLS LAMONT HANDAGES/MED WRAP DRESSINGS received FDA 510(k) clearance under submission number K925937, sponsored by Wells Lamont Corp.. 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 1993-08-09.

Classification & Regulation

This clearance is catalogued under FDA product code KMF and 21 CFR 880.5090, within the General Hospital review panel as a Class I device.