eCFR Reference Browser

---

title: "21 CFR §868.2500"

source: "https://www.ecfr.gov/current/title-21/section-868.2500"

title_number: "21"

volume_number: "8"

chapter_number: "Unknown"

subchapter_code: "H"

subchapter_subject: "MEDICAL DEVICES"

part_code: "868"

part_subject: "ANESTHESIOLOGY DEVICES"

subpart_code: "C"

subpart_subject: "Monitoring Devices"

section_number: "868.2500"

section_subject: "Cutaneous oxygen (PcO2) monitor."

cfr_reference: "21 CFR 868.2500"

title_name: "Title 21"

title_subject: "Food and Drugs"

parts_covered: "Parts 800 to 1299"

revised_date: "Revised as of April 1, 2019"

publication_date: "As of April 1, 2019"

contains_description: "Containing a codification of documents of general applicability and future effect"

publication_info: "Published by the Office of the Federal Register National Archives and Records Administration as a Special Edition of the Federal Register"

---

(a)Identification. A cutaneous oxygen (PcO2) monitor is a noninvasive, heated sensor (e.g., a Clark-type polargraphic electrode) placed on the patient's skin that is intended to monitor relative changes in the cutaneous oxygen tension.

(b)Classification. Class II (special controls). The special control for this device is FDA's “Class II Special Controls Guidance Document: Cutaneous Carbon Dioxide (PcCO2) and Oxygen (PcO2) Monitors; Guidance for Industry and FDA.” See § 868.1(e) for the availability of this guidance document.

§868.2500 - Cutaneous oxygen (PcO2) monitor.