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CASTLE & RITTER MINOR SURG. & EXAM LT

K811728 Class II Traditional
Decision Date
1981-07-20
Sponsor / Applicant
Sybron Corp.

Technical Specification

510(k) Submission ID K811728
Product Code FTD
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4580
Decision Date 1981-07-20
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CASTLE & RITTER MINOR SURG. & EXAM LT received FDA 510(k) clearance under submission number K811728, sponsored by Sybron Corp.. 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 1981-07-20.

Classification & Regulation

This clearance is catalogued under FDA product code FTD and 21 CFR 878.4580, within the General, Plastic Surgery review panel as a Class II device.