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STERILE CARBON STEEL SURGICAL BLADE

K900266 Class I Traditional
Decision Date
1990-03-01
Sponsor / Applicant
Rahn Laboratories

Technical Specification

510(k) Submission ID K900266
Product Code GES
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4800
Decision Date 1990-03-01
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

STERILE CARBON STEEL SURGICAL BLADE received FDA 510(k) clearance under submission number K900266, sponsored by Rahn Laboratories. The device was reviewed via the Traditional premarket notification pathway and assigned to the General, Plastic Surgery review panel. The statutory decision date of record is 1990-03-01.

Classification & Regulation

This clearance is catalogued under FDA product code GES and 21 CFR 878.4800, within the General, Plastic Surgery review panel as a Class I device.