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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