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FOAM CALCIUM ALIGINATE TOPICAL WOUND DRESSING

K963656 Class I Traditional
Decision Date
1996-11-12
Sponsor / Applicant
Adri

Technical Specification

510(k) Submission ID K963656
Product Code KMF
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5090
Decision Date 1996-11-12
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

FOAM CALCIUM ALIGINATE TOPICAL WOUND DRESSING received FDA 510(k) clearance under submission number K963656, sponsored by Adri. 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 1996-11-12.

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.