FDA 510(k) Applications for Medical Device Product Code "DQF"
(Actuator, Syringe, Injector Type)

FDA 510(k) Number Applicant Device Name Decision Date
K882723 ALCON LABORATORIES ALCON FLUID INJECTOR 11/08/1988
K920177 BIOTEQUE AMERICA, INC. VERSA-VIAL 07/13/1992
K880740 SPECTRAMED, INC. MODEL TA-CS10 SPECTRAJECT CONTROL SYRINGE 03/22/1988


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