FDA 21 CFR Part 895 Banned Devices

FDA 21 CFR Part 895 Banned Devices:

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Table of contents

Subpart A - General Provisions

895.1 Scope.

895.20 General.

895.21 Procedures for banning a device.

895.22 Submission of data and information by the manufacturer, distributor, or importer.

895.25 Labelling.

895.30 Special effective date.

Subpart B - Listing of Banned Devices

895.101 Prosthetic hair fibers.

895.102 Powdered surgeon's glove.

895.103 Powdered patient examination glove.

895.104 Absorbable powder for lubricating a surgeon's glove.

895.105 Electrical stimulation devices for self-injurious or aggressive behavior.

FDA 21 CFR Part 895 Banned Devices: