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BAXTER DISPOSABLE CIRCUMCISION TRAY

K884290 Class II Traditional
Decision Date
1988-12-08
Sponsor / Applicant
Baxter Healthcare Corp

Technical Specification

510(k) Submission ID K884290
Product Code HFX
Medical Specialty / Panel Obstetrics/Gynecology
Regulation Citation 21 CFR 884.4530
Decision Date 1988-12-08
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

BAXTER DISPOSABLE CIRCUMCISION TRAY received FDA 510(k) clearance under submission number K884290, sponsored by Baxter Healthcare 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 1988-12-08.

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.