FDA 510(k) Applications Submitted by PM DEVICES, INC.

FDA 510(k) Number Submission Date Device Name Applicant
K040835 03/31/2004 PERIPATCH SHEET, MODELS 1.5P8, 1.5P16, 4P4, 4P6, 6P8 AND 10P16 PM DEVICES, INC.
K031948 06/24/2003 PERIPATCH SHEET, MODELS 1.5P8, 4P4, 4P6, 6P8, 10P16, 1.5P16 PM DEVICES, INC.
K033985 12/23/2003 PERIPATCH SLEEVE, MODELS G35, E35, G45, E45, G60, E60, 5C6, 5C8, 5C10 PM DEVICES, INC.
K063556 11/27/2006 PERIPATCH ENDO-SLEEVE PM DEVICES, INC.


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