FDA 510(k) Applications Submitted by GULL LABORATORIES, INC.

FDA 510(k) Number Submission Date Device Name Applicant
K971857 05/20/1997 MUMPS IGG ELISA TESTY GULL LABORATORIES, INC.
K983541 10/09/1998 HSV 1+2 IGG ELISA TEST GULL LABORATORIES, INC.
K962343 06/18/1996 TOXO IGG ELISA TEST GULL LABORATORIES, INC.


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