Find 510K Clearence requests from to with applicant of device name containing

Your search returned 150,359 reports recieved

This is a beta research project using open FDA clearance data sets and is not for clinical use.


You are on page 1 of 15036

510(k) Number/Type
Applicant
Device
Advisory Committe
Date Received
Decision Date
More Info
K131170 COVIDIEN, FORMERLY VALLEYLAB, A DIVISION OF TYCO H SONICISION STERILIZATION TRAY General Hospital 2013-04-24 2013-08-28
K130853 CLARIANCE IDYS(TM) C Orthopedic 2013-03-28 2013-11-13
K130857 B. BRAUN MEDICAL, INC. PRONTOSAN WOUND GEL X Unknown 2013-03-28 2013-10-08
K130025 SONENDO, INC. SONENDO ENDOTHERAPY SYSTEM Dental 2013-01-03 2013-06-11
K123442 ICAD, INC. XOFT AXXENT CERVICAL APPLICATORS Radiology 2012-11-08 2013-02-27
K123297 BIOMET MANUFACTUTING CORP. COMPRESS SEGMENTAL HUMERAL REPLACEMENT SYSTEM Orthopedic 2012-10-22 2012-11-20
K122983 KARL STORZ ENDOSCOPY-AMERICA, INC. KSEA BIPOLAR ELECTRODE Obstetrics/Gynecology 2012-09-26 2013-06-26
K122870 CONFORMIS, INC. ITOTAL CRUCIATE RETAINING (CR) KNEE REPLACEMENT SYSTEM Orthopedic 2012-09-19 2013-01-14
K122702 FILLIGENT LIMITED BIOFRIEND BIOMASK N95 SURGICAL RESPIRATOR General, Plastic Surgery 2012-09-04 2013-03-18
K011122 RUSCH INTL. BALLPEN SPINAL NEEDLE W/WO INTRODUCER Anesthesiology 2001-04-12 2001-11-16

Click on any graph value to further filter your results

Please wait while we load the graphs.