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MARTIN TRACH-SECURE

K810575 Class II Traditional
Decision Date
1981-03-17
Sponsor / Applicant
Diatek, Inc.

Technical Specification

510(k) Submission ID K810575
Product Code BTO
Medical Specialty / Panel Anesthesiology
Regulation Citation 21 CFR 868.5800
Decision Date 1981-03-17
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MARTIN TRACH-SECURE received FDA 510(k) clearance under submission number K810575, sponsored by Diatek, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Anesthesiology review panel. The statutory decision date of record is 1981-03-17.

Classification & Regulation

This clearance is catalogued under FDA product code BTO and 21 CFR 868.5800, within the Anesthesiology review panel as a Class II device.