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EZ-CIRC

K963223 Class II Traditional
Decision Date
1997-04-23
Sponsor / Applicant
Phyllis Adams, Rn, Npc, Msn

Technical Specification

510(k) Submission ID K963223
Product Code HFW
Medical Specialty / Panel Obstetrics/Gynecology
Regulation Citation 21 CFR 884.4530
Decision Date 1997-04-23
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

EZ-CIRC received FDA 510(k) clearance under submission number K963223, sponsored by Phyllis Adams, Rn, Npc, Msn. 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 1997-04-23.

Classification & Regulation

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