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SURGICAL TOWEL CLIPS

K890231 Class I Traditional
Decision Date
1989-01-27
Sponsor / Applicant
Kinetic Medical Products

Technical Specification

510(k) Submission ID K890231
Product Code HBR
Medical Specialty / Panel Neurology
Regulation Citation 21 CFR 882.4215
Decision Date 1989-01-27
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SURGICAL TOWEL CLIPS received FDA 510(k) clearance under submission number K890231, sponsored by Kinetic Medical Products. The device was reviewed via the Traditional premarket notification pathway and assigned to the Neurology review panel. The statutory decision date of record is 1989-01-27.

Classification & Regulation

This clearance is catalogued under FDA product code HBR and 21 CFR 882.4215, within the Neurology review panel as a Class I device.