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U.S. Department of Health and Human Services

Medical Device Recalls

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1 to 3 of 3 Results
510(K) Number: K060550
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FDA Recall
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Kodak DirectView DR3000/3500 - Product Usage: permanently installed as a diagnostic system intended ... 2 01/13/2020 Carestream Health, Inc.
Kodak DirectView Model DR 3000 System, Stationary X-ray System; Catalog #s 6551360, 6551386, 6552152... 2 02/23/2008 Carestream Health, Inc.
Kodak Direct View DR3000 System, Stationary X-ray System, Catalog #s 655-1345, 655-1386. 2 07/03/2007 Carestream Health, Inc.