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Medical Devices; Ophthalmic Devices; Classification of the Hydrophilic Re-Coating Solution

fda-device · Food and Drug Administration · Rule · Published 2024-09-05 · Effective 2024-09-05 · 89 FR 72322

Document

Document number
2024-19882
Federal Register citation
89 FR 72322
CFR reference
21 CFR 886
Type
Rule
Action
Final amendment; final order.
Category
fda-device
Sub-agency
Food and Drug Administration
Publication date
2024-09-05
Effective date
2024-09-05
HHS docket
Docket No. FDA-2024-N-3970

Abstract

The Food and Drug Administration (FDA, Agency, or we) is classifying the hydrophilic re-coating solution into class II (special controls). The special controls that apply to the device type are identified in this order and will be part of the codified language for the hydrophilic re-coating solution's classification. We are taking this action because we have determined that classifying the device into class II (special controls) will provide a reasonable assurance of safety and effectiveness of the device. We believe this action will also enhance patients' access to beneficial innovative devices.

Source

Authoritative
Federal Register document
Machine
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