ClearanceBrief
510(k) K023019 ยท FGI Catheter, Urethrographic, Male

VOMED URETHRA OLIVE, MODELS 1420 000, 1425 000, 1430 000

ApplicantVomed Volzer Medizintechnik GmbH & Co., Hot Springs NC, US
DecisionSubstantially Equivalent, Dec 10, 2002
ReceivedSep 11, 2002
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K023019

No recall in the FDA data names this 510(k).

Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.