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FDA 510(k) Applications Submitted by CHESTNUT MEDICAL TECHNOLOGIES, INC.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K043580
12/28/2004
ALLIGATOR RETRIEVAL DEVICE (ARD)
CHESTNUT MEDICAL TECHNOLOGIES, INC.
K091559
05/28/2009
MARKSMANN CATHETER
CHESTNUT MEDICAL TECHNOLOGIES, INC.
K093977
12/24/2009
ALLIGATOR-HD RETRIEVAL DEVICE (ARD-HD), MODEL FA-88840-XX
CHESTNUT MEDICAL TECHNOLOGIES, INC.
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