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SALTER LABS MODEL #4009 SAMPLE LINES

K894350 Class II Traditional
Decision Date
1989-10-03
Sponsor / Applicant
Salter Labs

Technical Specification

510(k) Submission ID K894350
Product Code CCK
Medical Specialty / Panel Anesthesiology
Regulation Citation 21 CFR 868.1400
Decision Date 1989-10-03
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SALTER LABS MODEL #4009 SAMPLE LINES received FDA 510(k) clearance under submission number K894350, sponsored by Salter Labs. The device was reviewed via the Traditional premarket notification pathway and assigned to the Anesthesiology review panel. The statutory decision date of record is 1989-10-03.

Classification & Regulation

This clearance is catalogued under FDA product code CCK and 21 CFR 868.1400, within the Anesthesiology review panel as a Class II device.