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IN-SIGHT SURGICAL INSTRUMENT KITS, DISPOSABLE

K910816 Class I Traditional
Decision Date
1991-04-17
Sponsor / Applicant
Insight International, Inc.

Technical Specification

510(k) Submission ID K910816
Product Code KDD
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4800
Decision Date 1991-04-17
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

IN-SIGHT SURGICAL INSTRUMENT KITS, DISPOSABLE received FDA 510(k) clearance under submission number K910816, sponsored by Insight International, Inc.. 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 1991-04-17.

Classification & Regulation

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