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I.V. TAPE DOWN HOLDER

K800024 Class I Traditional
Decision Date
1980-01-29
Sponsor / Applicant
Consolidated Medical Equipment, Inc.

Technical Specification

510(k) Submission ID K800024
Product Code KMK
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5210
Decision Date 1980-01-29
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

I.V. TAPE DOWN HOLDER received FDA 510(k) clearance under submission number K800024, sponsored by Consolidated Medical Equipment, 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 1980-01-29.

Classification & Regulation

This clearance is catalogued under FDA product code KMK and 21 CFR 880.5210, within the General Hospital review panel as a Class I device.