EDSLAB(R) DUAL LUMEN REGION SATUR OXIMETRY CATH— 510(k) K926450

Name: FDA 510(k) clearance K926450
Creator: U.S. Food and Drug Administration
Published: 1993-02-22

Substantially Equivalent

Baxter Healthcare Corp

FDA 510(k) clearance K926450 for EDSLAB(R) DUAL LUMEN REGION SATUR OXIMETRY CATH, Substantially Equivalent on 1993-02-22. Applicant: Baxter Healthcare Corp. Device class: 2.

Clearance details

Applicant: Baxter Healthcare Corp
Product code: Code DQE
Device class: Class 2
Regulation: 21 CFR 870.1230
Advisory panel: Cardiovascular
Date received: 1992-12-24
Decision date: 1993-02-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Santa Ana, CA, US

Download summary PDF View on FDA.gov ↗

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