yourstate.us
21 CFR 862.1460

§ 862.1460 Leucine aminopeptidase test system.

United States · 21 CFR — Food and Drugs · Status: effective

Get this as JSONEmbed this
Cite this
Citation
21 CFR 862.1460, § 862.1460 Leucine aminopeptidase test system, United States, version 1 as recorded 2026-07-09, yourstate.us, https://yourstate.us/provision/89135
Permanent ID
ys:prov:89135@1
SHA-256
014ab8f52ece4fde9daf7394085fdda604491897ac8c70ccc18dd6888b9bd1e9

The hash is SHA-256 of this version's text, with every run of whitespace collapsed to a single space and the ends trimmed. The ID always leads back here, and checking it says whether the text you cited is still the current version.

Full text

(a) Identification. A leucine aminopeptidase test system is a device intended to measure the activity of the enzyme leucine amino-peptidase in serum, plasma, and urine. Leucine aminopeptidase measurements are used in the diagnosis and treatment of liver diseases such as viral hepatitis and obstructive jaundice. (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.

Legislative history

This is a federal regulation, adopted through agency rulemaking under the Administrative Procedure Act — not enacted by a recorded vote of Congress.