# Hematology and Pathology Devices; Reclassification; Restricted Devices; OTC Test Sample Collection Systems for Drugs of Abuse Testing; Delay of Effective Date
> **Food and Drug Administration** · Final rule; delay of effective date. · Published 2001-03-30 · Effective 2000-04-07 · 66 FR 17359
## Document
- **Document number:** 01-7833
- **Category:** other
- **Sub-agency:** Food and Drug Administration
- **Federal Register citation:** 66 FR 17359
- **CFR reference:** 21 CFR 809
- **Publication date:** 2001-03-30
- **Effective date:** 2000-04-07
- **HHS docket:** Docket No. 97N-0135
## Abstract

In accordance with the memorandum of January 20, 2001, from the Assistant to the President and Chief of Staff, entitled "Regulatory Review Plan," published in the Federal Register on January 24, 2001 (66 FR 7702), this action temporarily delays for 60 days the effective date of the rule entitled "Hematology and Pathology Devices; Reclassification; Restricted Devices; OTC Test Sample Collection Systems for Drugs of Abuse Testing," published in the Federal Register on April 7, 2000 (65 FR 18230).

## Source
- [Federal Register document](https://www.federalregister.gov/documents/2001/03/30/01-7833/hematology-and-pathology-devices-reclassification-restricted-devices-otc-test-sample-collection)
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