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CENTURION CIRCLAMP

K890897 Class II Traditional
Decision Date
1989-03-28
Sponsor / Applicant
Tri-State Hospital Supply Corp.

Technical Specification

510(k) Submission ID K890897
Product Code HFX
Medical Specialty / Panel Obstetrics/Gynecology
Regulation Citation 21 CFR 884.4530
Decision Date 1989-03-28
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CENTURION CIRCLAMP received FDA 510(k) clearance under submission number K890897, sponsored by Tri-State Hospital Supply Corp.. 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 1989-03-28.

Classification & Regulation

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