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PLASTIC LEG BAG

K831530 Class II Traditional
Decision Date
1984-01-03
Sponsor / Applicant
Forever-Dry, Inc.

Technical Specification

510(k) Submission ID K831530
Product Code KNX
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.5250
Decision Date 1984-01-03
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PLASTIC LEG BAG received FDA 510(k) clearance under submission number K831530, sponsored by Forever-Dry, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Gastroenterology, Urology review panel. The statutory decision date of record is 1984-01-03.

Classification & Regulation

This clearance is catalogued under FDA product code KNX and 21 CFR 876.5250, within the Gastroenterology, Urology review panel as a Class II device.