510(k) K101873 · BZG Spirometer, Diagnostic

MASTERSCREEN IOS

Applicant	Carefusion Germany 234 GmbH, Hoechberg, DE
Decision	Substantially Equivalent, Feb 10, 2011
Received	Jul 6, 2010
Type	Traditional
FDA record	Open on fda.gov

Recalls that name K101873

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.