FDA 510(k) Applications Submitted by MID-ATLANTIC DIAGNOSTICS, INC.

FDA 510(k) Number Submission Date Device Name Applicant
K100596 03/02/2010 CRYOPETTE MID-ATLANTIC DIAGNOSTICS, INC.
K030525 02/19/2003 CUSTOM PRODUCTS IVF WORKSTATION TYPE WKST-24*36, WKST-24*48, WKST-24*60, WKST-24*72 AND WKST-24*72D PLUS ACCESSORIES MID-ATLANTIC DIAGNOSTICS, INC.
K041435 05/28/2004 THE STRIPPER PGD MID-ATLANTIC DIAGNOSTICS, INC.
K993699 11/02/1999 THE STRIPPER MID-ATLANTIC DIAGNOSTICS, INC.


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