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FDA 510(k) Applications Submitted by GRACE CARLSON
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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