510(k) K001688 · DQA Oximeter

DATEX-OHMEDA TUFFSAT 3000 PULSE OXIMETER

Applicant	Datex-Ohmeda, Inc., Louisville CO, US
Decision	Substantially Equivalent, Jun 30, 2000
Received	Jun 2, 2000
Type	Special
FDA record	Open on fda.gov

Recalls that name K001688

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.