meddevicedb.com FDA Device Reference

WOMEN AND INFANT'S DELIVERY PACK

K912869 Class II Traditional
Decision Date
1991-12-04
Sponsor / Applicant
Welcon, Inc.

Technical Specification

510(k) Submission ID K912869
Product Code HFW
Medical Specialty / Panel Obstetrics/Gynecology
Regulation Citation 21 CFR 884.4530
Decision Date 1991-12-04
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

WOMEN AND INFANT'S DELIVERY PACK received FDA 510(k) clearance under submission number K912869, sponsored by Welcon, 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 1991-12-04.

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.