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FDA 510(k) Applications Submitted by JOHN D'ANGELO
FDA 510(k) Number
Submission Date
Device Name
Applicant
K020374
02/04/2002
OCULIGHT SL/SLX
IRIDEX CORP.
K020849
03/15/2002
APEX 800 LASER SYSTEM, MODEL APEX 800
IRIDEX CORP.
K981266
04/07/1998
AUTO-INJECTOR, SURE-INJECT 2000
MIGHTY MO, CORP.
K022228
07/10/2002
FAMILY OF IRIS MEDICAL ENDOPROBE HANDPIECES
IRIDEX CORP.
K982816
08/11/1998
VNUS CLOSURE SYSTEM
VNUS MEDICAL TECHNOLOGIES, INC.
K082562
09/04/2008
APPLIED BIOSYSTEMS 7500 FAST DX
APPLIED BIOSYSTEMS INC
K993900
11/16/1999
COAGULATION ELECTRODE, MODEL 2000; RADIOFREQUENCY GENERATOR, MODEL 20-115
BRONCUS TECHNOLOGIES, INC.
K955594
12/08/1995
SAFELINE I.V. BAG ACCESS DEVICE
MCGAW, INC.
K955595
12/08/1995
SAFELINE MULTIDOSE VIAL ADAPTER
MCGAW, INC.
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