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PALCO LABS MODEL 340 PULSE OXIMETER

K920066 Class II Traditional
Decision Date
1993-03-16
Sponsor / Applicant
Palco Laboratories, Inc.

Technical Specification

510(k) Submission ID K920066
Product Code DQA
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.2700
Decision Date 1993-03-16
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PALCO LABS MODEL 340 PULSE OXIMETER received FDA 510(k) clearance under submission number K920066, sponsored by Palco Laboratories, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 1993-03-16.

Classification & Regulation

This clearance is catalogued under FDA product code DQA and 21 CFR 870.2700, within the Cardiovascular review panel as a Class II device.