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SURGICAL TROCAR

K911462 Class II Traditional
Decision Date
1991-04-22
Sponsor / Applicant
Applied Medical

Technical Specification

510(k) Submission ID K911462
Product Code DRC
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.1390
Decision Date 1991-04-22
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SURGICAL TROCAR received FDA 510(k) clearance under submission number K911462, sponsored by Applied Medical. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 1991-04-22.

Classification & Regulation

This clearance is catalogued under FDA product code DRC and 21 CFR 870.1390, within the Cardiovascular review panel as a Class II device.