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SONOSURE SONOHYSTEROGRAPHY & ENDOMETRIAL SAMPLING DEVICE

K133144 Class II Traditional
Decision Date
2014-03-19
Sponsor / Applicant
Crossbay Medical, Inc.

Technical Specification

510(k) Submission ID K133144
Product Code PGK
Medical Specialty / Panel Obstetrics/Gynecology
Regulation Citation 21 CFR 884.4530
Decision Date 2014-03-19
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SONOSURE SONOHYSTEROGRAPHY & ENDOMETRIAL SAMPLING DEVICE received FDA 510(k) clearance under submission number K133144, sponsored by Crossbay Medical, 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 2014-03-19.

Classification & Regulation

This clearance is catalogued under FDA product code PGK and 21 CFR 884.4530, within the Obstetrics/Gynecology review panel as a Class II device.