meddevicedb.com FDA Device Reference

SECU-TAPE UNIVERSAL FLEXIBLE MEDICAL CLAMPS

K850503 Class I Traditional
Decision Date
1985-04-01
Sponsor / Applicant
Turn Needle Intl., Inc.

Technical Specification

510(k) Submission ID K850503
Product Code KMK
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5210
Decision Date 1985-04-01
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SECU-TAPE UNIVERSAL FLEXIBLE MEDICAL CLAMPS received FDA 510(k) clearance under submission number K850503, sponsored by Turn Needle Intl., 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 1985-04-01.

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.