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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