FDA 510(k) Applications Submitted by GRACE CARLSON, MD

FDA 510(k) Number Submission Date Device Name Applicant
K082786 09/23/2008 PULSAR GENERATOR, PEAK PLASMABLADE; 4.0, NEEDLE, AND EXT TISSUE DISSECTION DEVICES PEAK SURGICAL, INC.
K073057 10/30/2007 PULSAR GENERATOR, MODEL PS100-100, AND PEAK PLASMABLADE TISSUE DISSECTION DEVICE, MODEL PS200-040 PEAK SURGICAL, INC.
K132669 08/27/2013 PROXIFAST ABSORBABLE STAPLE SURGIMATIX, INC.


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