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UMI DISPOSABLE BUTTERFLY STYLE PUNCTURE NEEDLE

K881796 Class I Traditional
Decision Date
1988-07-26
Sponsor / Applicant
Universal Medical Instrument Corp.

Technical Specification

510(k) Submission ID K881796
Product Code DWS
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.4500
Decision Date 1988-07-26
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

UMI DISPOSABLE BUTTERFLY STYLE PUNCTURE NEEDLE received FDA 510(k) clearance under submission number K881796, sponsored by Universal Medical Instrument Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 1988-07-26.

Classification & Regulation

This clearance is catalogued under FDA product code DWS and 21 CFR 870.4500, within the Cardiovascular review panel as a Class I device.