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DOMAIN SURGICAL SYSTEM

K121881 Class II Traditional
Decision Date
2012-10-18
Sponsor / Applicant
Domain Surgical, Inc.

Technical Specification

510(k) Submission ID K121881
Product Code HGI
Medical Specialty / Panel Obstetrics/Gynecology
Regulation Citation 21 CFR 884.4120
Decision Date 2012-10-18
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

DOMAIN SURGICAL SYSTEM received FDA 510(k) clearance under submission number K121881, sponsored by Domain Surgical, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Obstetrics/Gynecology review panel. The statutory decision date of record is 2012-10-18.

Classification & Regulation

This clearance is catalogued under FDA product code HGI and 21 CFR 884.4120, within the Obstetrics/Gynecology review panel as a Class II device.