eCFR Reference Browser

---

title: "21 CFR §884.1630"

source: "https://www.ecfr.gov/current/title-21/section-884.1630"

title_number: "21"

volume_number: "8"

chapter_number: "Unknown"

subchapter_code: "H"

subchapter_subject: "MEDICAL DEVICES"

part_code: "884"

part_subject: "OBSTETRICAL AND GYNECOLOGICAL DEVICES"

subpart_code: "B"

subpart_subject: "Obstetrical and Gynecological Diagnostic Devices"

section_number: "884.1630"

section_subject: "Colposcope."

cfr_reference: "21 CFR 884.1630"

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 colposcope is a device designed to permit direct viewing of the tissues of the vagina and cervix by a telescopic system located outside the vagina. It is used to diagnose abnormalities and select areas for biopsy. This generic type of device may include a light source, cables, and component parts.

(b)Classification. Class II (performance standards).

§884.1630 - Colposcope.