21 CFR § 876.1300 - Ingestible telemetric gastrointestinal capsule imaging system.
---
identifier: "/us/cfr/t21/s876.1300"
source: "ecfr"
legal_status: "authoritative_unofficial"
title: "21 CFR § 876.1300 - Ingestible telemetric gastrointestinal capsule imaging system."
title_number: 21
title_name: "Food and Drugs"
section_number: "876.1300"
section_name: "Ingestible telemetric gastrointestinal capsule imaging system."
chapter_name: "FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES"
subchapter_number: "H"
subchapter_name: "MEDICAL DEVICES"
part_number: "876"
part_name: "GASTROENTEROLOGY-UROLOGY DEVICES"
positive_law: false
currency: "2026-04-05"
last_updated: "2026-04-05"
format_version: "1.1.0"
generator: "[email protected]"
authority: "21 U.S.C. 351, 360, 360c, 360e, 360j, 360 371."
regulatory_source: "48 FR 53023, Nov. 23, 1983, unless otherwise noted."
cfr_part: "876"
---
# 876.1300 Ingestible telemetric gastrointestinal capsule imaging system.
(a) *Identification.* An ingestible telemetric gastrointestinal capsule imaging system is used for visualization of the small bowel mucosa as an adjunctive tool in the detection of abnormalities of the small bowel. The device captures images of the small bowel with a wireless camera contained in a capsule. This device includes an ingestible capsule (containing a light source, camera, transmitter, and battery), an antenna array, a receiving/recording unit, a data storage device, computer software to process the images, and accessories.
(b) *Classification.* Class II (special controls). The special control is FDA's guidance, “Class II Special Controls Guidance Document: Ingestible Telemetric Gastrointestinal Capsule Imaging Systems; Final Guidance for Industry and FDA.”
[67 FR 3433, Jan. 24, 2002]