FDA 510(k) Applications Submitted by Donald Henton
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K110268 |
01/28/2011 |
FORCETRIAD ELECTROSURGICAL GENERATOR |
COVIDIEN LP, FORMERLY KNOW AS VALLEYLAB, A DIVISON |
| K030464 |
02/12/2003 |
GEM, MODEL 004110 |
COLLINS MEDICAL, INC. |
| K030917 |
03/24/2003 |
GEM; HAWK; EAGLE; MODELS 004110, 0044120, 004130 |
COLLINS MEDICAL, INC. |
| K051572 |
06/14/2005 |
KOKO LEGEND |
PULMONARY DATA SERVICES, INC. |
| K172509 |
08/21/2017 |
Sentosa SA201 HSV 1/2 Qualitative PCR Test |
Vela Diagnostics USA Inc. |
| K982956 |
08/24/1998 |
FLOWMATE II PLUS, MODEL #4000 |
SPIROMETRICS MEDICAL EQUIPMENT CO. |
| K954759 |
10/17/1995 |
FLOWMATE LTE |
SPIROMETRICS MEDICAL EQUIPMENT CO. |
| K133338 |
10/30/2013 |
LIGASURE 5 MM MARYLAND JAW SEALER/DIVIDER ONE-STEP SEALING (LF 17XX) |
COVIDIEN, FORMERLY VALLEYLAB, A DIVISION OF TYCO H |
| K143654 |
12/23/2014 |
Valleylab LS10 Generator |
COVIDIEN LLC |
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