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BUTTERFLY DRESSING

K912160 Class I Traditional
Decision Date
1991-10-09
Sponsor / Applicant
Durden Enterprises, Inc.

Technical Specification

510(k) Submission ID K912160
Product Code KGX
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5240
Decision Date 1991-10-09
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

BUTTERFLY DRESSING received FDA 510(k) clearance under submission number K912160, sponsored by Durden Enterprises, 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 1991-10-09.

Classification & Regulation

This clearance is catalogued under FDA product code KGX and 21 CFR 880.5240, within the General Hospital review panel as a Class I device.