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TOCOLYTIC SITE CARE SUP KIT #1001/100A/CARRY CASE

K893003 Class II Traditional
Decision Date
1989-07-14
Sponsor / Applicant
United Medical Systems, Inc.

Technical Specification

510(k) Submission ID K893003
Product Code FOZ
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5200
Decision Date 1989-07-14
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

TOCOLYTIC SITE CARE SUP KIT #1001/100A/CARRY CASE received FDA 510(k) clearance under submission number K893003, sponsored by United Medical Systems, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the General Hospital review panel. The statutory decision date of record is 1989-07-14.

Classification & Regulation

This clearance is catalogued under FDA product code FOZ and 21 CFR 880.5200, within the General Hospital review panel as a Class II device.