21 CFR 884.1050
§ 884.1050 Endocervical aspirator.
United States · 21 CFR — Food and Drugs · Status: effective
Cite this
- Citation
- 21 CFR 884.1050, § 884.1050 Endocervical aspirator, United States, version 1 as recorded 2026-07-09, yourstate.us, https://yourstate.us/provision/90778
- Permanent ID
ys:prov:90778@1- SHA-256
5ef800af5ef27e8841a1794ab1153f4401ea4fd80d0ffc04d34f60c4039ee308
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. An endocervical aspirator is a device designed to remove tissue from the endocervix (mucous membrane lining the canal of the cervix of the uterus) by suction with a syringe, bulb and pipette, or catheter. This device is used to evaluate endocervical tissue to detect malignant and premalignant lesions.
(b) Classification. Class II (performance standards).
Legislative history
This is a federal regulation, adopted through agency rulemaking under the Administrative Procedure Act — not enacted by a recorded vote of Congress.