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MEDLINE CIRCUMCISION TRAY

K970282 Class II Traditional
Decision Date
1997-03-06
Sponsor / Applicant
Medline

Technical Specification

510(k) Submission ID K970282
Product Code HFX
Medical Specialty / Panel Obstetrics/Gynecology
Regulation Citation 21 CFR 884.4530
Decision Date 1997-03-06
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MEDLINE CIRCUMCISION TRAY received FDA 510(k) clearance under submission number K970282, sponsored by Medline. 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 1997-03-06.

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.