Atlas FDA

Peak Surgical, Inc.

7 FDA 510(k) clearances · Manufacturer

Sort:Newest firstOldest first

Export predicate table (CSV) Shareable report ◉ Watch exports: 3 free/month · reports & watching: free

RecordFirmDate
PEAK SUCTION COAGULATOR (K103775)Peak Surgical, Inc.2011-05-27
PEAK PLASMABLADE PLUS TISSUE DISSECTION DEVICE (K102709)Peak Surgical, Inc.2010-12-17
PEAK PULSAR II GENERATOR MODEL PS100-102 (K102029)Peak Surgical, Inc.2010-12-16
PEAK PLASMABLADE 3.OS TISSUE DISSECTION DEVICE (K093695)Peak Surgical, Inc.2010-04-13
PEAK PLASMABLADE TNA TONSIL AND ADENOID TISSUE DISSECTION DEVICE (K083415)Peak Surgical, Inc.2009-06-05
PULSAR GENERATOR, PEAK PLASMABLADE; 4.0, NEEDLE, AND EXT TISSUE DISSECTION DEVICES (K082786)Peak Surgical, Inc.2008-12-03
PULSAR GENERATOR, MODEL PS100-100, AND PEAK PLASMABLADE TISSUE DISSECTION DEVICE, MODEL PS200-040 (K073057)Peak Surgical, Inc.2008-07-22

Track Peak Surgical, Inc. automatically

Every clearance here is in the API, with alerts when new ones post.