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EXUSORB(TM) DRY/WET DRESSING

K896176 Class I Traditional
Decision Date
1989-11-24
Sponsor / Applicant
Controlled Therapeutics Corp.

Technical Specification

510(k) Submission ID K896176
Product Code KOZ
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4018
Decision Date 1989-11-24
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

EXUSORB(TM) DRY/WET DRESSING received FDA 510(k) clearance under submission number K896176, sponsored by Controlled Therapeutics Corp.. 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 1989-11-24.

Classification & Regulation

This clearance is catalogued under FDA product code KOZ and 21 CFR 878.4018, within the General, Plastic Surgery review panel as a Class I device.