{"data":{"id":"us/21-cfr-880.2420","jurisdiction":"us","citation":"21 CFR 880.2420","heading":"Electronic monitor for gravity flow infusion systems.","body":"(a) Identification. An electronic monitor for gravity flow infusion systems is a device used to monitor the amount of fluid being infused into a patient. The device consists of an electronic transducer and equipment for signal amplification, conditioning, and display.\n(b) Classification. Class II (performance standards).","path":["Title 21—Food and Drugs","CHAPTER I—FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES","SUBCHAPTER H—MEDICAL DEVICES","PART 880—GENERAL HOSPITAL AND PERSONAL USE DEVICES","Subpart C—General Hospital and Personal Use Monitoring Devices"],"source_url":"https://www.ecfr.gov/api/versioner/v1/full/2026-08-25/title-21.xml","current_through":"2026-08-25","vintage":"","retrieved_at":"2026-08-27T02:24:47Z","sha256":"7c20a46bb8f8a6224415781d01305295e7d349f7eae25ced1886d9cc8f9dba40","source_id":"us-cfr","stale":true,"prev":"us/21-cfr-880.2400","next":"us/21-cfr-880.2460"},"notice":"GroundRules: Original legal text. Not legal advice."}