FDA 21 CFR Part 895 Banned Devices:
Table of contents
Subpart A - General Provisions
895.21 Procedures for banning a device.
895.22 Submission of data and information by the manufacturer, distributor, or importer.
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:
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