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KOREAN GREEN CROSS SCALP VEIN SET

K862289 Class II Traditional
Decision Date
1986-09-23
Sponsor / Applicant
Sturbridge Medical

Technical Specification

510(k) Submission ID K862289
Product Code FPA
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5440
Decision Date 1986-09-23
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

KOREAN GREEN CROSS SCALP VEIN SET received FDA 510(k) clearance under submission number K862289, sponsored by Sturbridge Medical. 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 1986-09-23.

Classification & Regulation

This clearance is catalogued under FDA product code FPA and 21 CFR 880.5440, within the General Hospital review panel as a Class II device.