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STERILE IMPERVIOUS ORTHOPEDIC STOCKIN

K792357 Class II Traditional
Decision Date
1979-12-18
Sponsor / Applicant
Alba-Waldensian, Inc.

Technical Specification

510(k) Submission ID K792357
Product Code KKX
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4370
Decision Date 1979-12-18
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

STERILE IMPERVIOUS ORTHOPEDIC STOCKIN received FDA 510(k) clearance under submission number K792357, sponsored by Alba-Waldensian, Inc.. 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 1979-12-18.

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.