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STERILE SURGICAL BLADES

K852141 Class I Traditional
Decision Date
1985-06-13
Sponsor / Applicant
Miltex Instrument Co.

Technical Specification

510(k) Submission ID K852141
Product Code GES
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4800
Decision Date 1985-06-13
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

STERILE SURGICAL BLADES received FDA 510(k) clearance under submission number K852141, sponsored by Miltex Instrument Co.. 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 1985-06-13.

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.