{"data":{"id":"us/21-cfr-862.2750","jurisdiction":"us","citation":"21 CFR 862.2750","heading":"Pipetting and diluting system for clinical use.","body":"(a) Identification. A pipetting and diluting system for clinical use is a device intended to provide an accurately measured volume of liquid at a specified temperature for use in certain test procedures. This generic type of device system includes serial, manual, automated, and semi-automated dilutors, pipettors, dispensers, and pipetting stations.\n(b) Classification. Class I (general controls). The device is exempt from the premarket notification procedures in subpart E of part 807 of this chapter subject to § 862.9.","path":["Title 21—Food and Drugs","CHAPTER I—FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES","SUBCHAPTER H—MEDICAL DEVICES","PART 862—CLINICAL CHEMISTRY AND CLINICAL TOXICOLOGY DEVICES","Subpart C—Clinical Laboratory Instruments"],"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":"a03e9cdb8233fc5bc3c2cd5c00e7d4e9b4e83fcaa7a8f12065a5ce4e48f036e7","source_id":"us-cfr","stale":true,"prev":"us/21-cfr-862.2730","next":"us/21-cfr-862.2800"},"notice":"GroundRules: Original legal text. Not legal advice."}