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OXIMETRIX SHAW HEMOSTATIC SURG. SYS.

K791868 Class II Traditional
Decision Date
1980-01-04
Sponsor / Applicant
Oximetrix, Inc.

Technical Specification

510(k) Submission ID K791868
Product Code GEI
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4400
Decision Date 1980-01-04
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

OXIMETRIX SHAW HEMOSTATIC SURG. SYS. received FDA 510(k) clearance under submission number K791868, sponsored by Oximetrix, 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 1980-01-04.

Classification & Regulation

This clearance is catalogued under FDA product code GEI and 21 CFR 878.4400, within the General, Plastic Surgery review panel as a Class II device.