June 14, 1999
6/14/99 Cardiopulmonary Corporation 59 units. Class II Venturi Ventilator with hard drive. User interface software will not load when unit is first powered on. Z-1039-9
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What’s New

FDA:  Exemptions, Variances, and Alternate Forms of Adverse Event Reporting for Medical Devices

Manufacturers, importers, and user facilities can request an exemption or variance from any or all of the medical device reporting requirements in 21 CFR Part 803.  Read more:

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