# Medical Devices; Exemptions From Premarket Notification: Class II Devices; Clinical Electronic Thermometers
> **Food and Drug Administration** · Final amendment; final Order. · Published 2025-06-18 · Effective 2025-06-18 · 90 FR 25889
## Document
- **Document number:** 2025-11207
- **Category:** fda-device
- **Sub-agency:** Food and Drug Administration
- **Federal Register citation:** 90 FR 25889
- **CFR reference:** 21 CFR 880
- **Publication date:** 2025-06-18
- **Effective date:** 2025-06-18
- **HHS docket:** Docket No. FDA-2023-N-4372
## Abstract

The Food and Drug Administration (FDA, we, or the Agency) is publishing an order setting forth the Agency's final determination to exempt certain class II clinical electronic thermometers from premarket notification (510(k)) requirements, subject to certain limitations. This exemption from 510(k), subject to certain limitations, is immediately in effect for such class II clinical electronic thermometers. This exemption will decrease regulatory burdens on the medical device industry and will eliminate private costs and expenditures required to comply with Federal regulations. FDA is amending the classification language within the Code of Federal Regulations for certain class II clinical electronic thermometers to reflect this final determination. FDA is publishing this order in accordance with the Federal Food, Drug, and Cosmetic Act (FD&C Act).

## Source
- [Federal Register document](https://www.federalregister.gov/documents/2025/06/18/2025-11207/medical-devices-exemptions-from-premarket-notification-class-ii-devices-clinical-electronic)
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