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TAMPER EVIDENT ARROWS WITH AND WITHOUT STERILIZATION INDICATORS

K951703 Class II Traditional
Decision Date
1995-06-28
Sponsor / Applicant
Products For Medicine

Technical Specification

510(k) Submission ID K951703
Product Code LRT
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.2800
Decision Date 1995-06-28
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

TAMPER EVIDENT ARROWS WITH AND WITHOUT STERILIZATION INDICATORS received FDA 510(k) clearance under submission number K951703, sponsored by Products For Medicine. 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 1995-06-28.

Classification & Regulation

This clearance is catalogued under FDA product code LRT and 21 CFR 880.2800, within the General Hospital review panel as a Class II device.