ClearanceBrief
510(k) K002343 ยท CAD Vaporizer, Anesthesia, Non-Heated

SIGMA DELTA

ApplicantPenlon , Ltd., Barton Lane, Abingdon, GB
DecisionSubstantially Equivalent, Jun 8, 2001
ReceivedAug 1, 2000
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K002343

DateFirm and productCodeLinked 510(k)
Jul 2, 2013Penlon, Ltd.
Delta Vaporizer An anesthetic vaporizer is a device used to vaporize liquid anesthetic and deliver a controlled amount of the vapor to the patient.
Terminated
CADNone listed

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