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FDA 510(k) Applications Submitted by HARRY SCHLAKMAN
FDA 510(k) Number
Submission Date
Device Name
Applicant
K990389
02/08/1999
MOSS GASTROSTOMY TUBE
MOSS TUBES, INC.
K984628
12/30/1998
MODIFICATION OF MOSS P.E.G. TRAY
MOSS TUBES, INC.
K984629
12/30/1998
MOSS TUBES, INC. NASAL TUBE - MARK IV
MOSS TUBES, INC.
K954112
07/31/1995
VYGON LIFEVAC MID-LINE TRAY
VYGON CORP.
K954302
09/13/1995
VYGON PREMI-CATH - LONG TERM CATHETER
VYGON CORP.
K984310
12/02/1998
MOSS TUBES, INC, ALL SILICONE GASTROSTOMY TUBE
MOSS TUBES, INC.
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