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PubMed

Medical Devices; Exemptions From Premarket Notification: Class II Devices. Final order.

PMID: 30019871 ·

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RevistaFederal register
Año
PMID30019871

Resumen

The Food and Drug Administration (FDA or the Agency) is publishing an order to exempt a list of class II devices from premarket notification (510(k)) requirements, subject to certain limitations. This exemption from 510(k), subject to certain limitations, is immediately in effect for the listed class II devices. This exemption will decrease regulatory burdens on the medical device industry and will eliminate private costs and expenditures required to comply with certain Federal regulations. FDA

Fuente oficial

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