510(k) K000369 · FMI Needle, Hypodermic, Single Lumen

VACUFLOW+ BLOOD COLLECTION SET, MODEL 52221/3/5; VACUFLOW+ WITH HOLDER BLOOD COLLECTION SET, MODEL 82021/3/5 WITH HOLDER

Applicant	Medpro Technologies, Inc., Appollo Beach FL, US
Decision	Substantially Equivalent, Mar 30, 2000
Received	Feb 4, 2000
Type	Traditional
FDA record	Open on fda.gov

Recalls that name K000369

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.