Devices & Diagnostics Letter
Feb. 20, 2012
| Vol.
39 No.
8
Proposed Rule Reclassifies Poison Treatment Tool
The FDA is slowly paring its list of devices grandfathered in under the 1976 medical device amendments, issuing a proposed rule to down-classify sorbent hemoperfusion devices for poisoning and drug overdose to Class II with special controls.
This article is viewable by subscribers only. To view this article, please select an option below.
|