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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