FDA 510(k) Applications Submitted by MERCEDES BAYANI
FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
K200262 |
02/03/2020 |
L100 Go System |
Bioness Inc. |
K190285 |
02/11/2019 |
L300 Go System |
Bioness Inc. |
K031079 |
04/04/2003 |
EVEREST BIPOLAR NEEDLE ELECTRODE & GYRUS BIPOLAR NEEDLE ELECTRODE |
GYRUS MEDICAL, INC. |
K031081 |
04/04/2003 |
EVEREST LP BIPOLAR SCISSORS AND GYRUS LP BIPOLAR SCISSORS |
GYRUS MEDICAL, INC. |
K031085 |
04/04/2003 |
GYRUS PLASMAKINETIC SUPERPULSE SYSTEM (GENERATOR, ACCESSORIES) |
GYRUS MEDICAL, INC. |
K191587 |
06/14/2019 |
L360 Thigh System |
Bioness Inc. |
K162407 |
08/29/2016 |
L300 Go System |
BIONESS INC. |
K173682 |
12/01/2017 |
L300 Go System |
Bioness, Inc. |
K951440 |
03/29/1995 |
LLC-MK2 (MONKEY KIDNEY, MACACA MULATA) CELL CULTURE |
VIROMED LABORATORIES, INC. |
K031078 |
04/04/2003 |
EVEREST BIPOLAR MACRO, MICRO & MOLLY FORCEPS & GYRUS BIPOLAR MACRO, MICRO & MOLLY FORCEPS |
GYRUS MEDICAL, INC. |
K031082 |
04/04/2003 |
EVEREST BIPOLAR L HOOK & PK BIPOLAR L HOOK |
GYRUS MEDICAL, INC. |
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