ClearanceBrief
510(k) K001430 ยท BTL Ventilator, Emergency, Powered (Resuscitator)

RESPIRTECH PRO-O2C, MODEL 2200 AND RESPIRTECH PRO, MODEL 2000

ApplicantVortran Medical Technology 1, Inc., Sacramento CA, US
DecisionSubstantially Equivalent, Jul 5, 2000
ReceivedMay 5, 2000
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K001430

DateFirm and productCodeLinked 510(k)
Apr 25, 2017Vortran Medical Technology 1, Inc
VORTRAN Automatic Resuscitator, VARPlus; Model PTE-5002; Qty: 10 each Anesthesiology: This device is to be used by properly trained personnel to deliver emergency, short term, constant flow, pressure
Terminated
BTLNone listed
Apr 25, 2017Vortran Medical Technology 1, Inc
VORTRAN Automatic Resuscitator, VARPlus with Extension Kit; Model PCE-5012; Qty: 10 each. Anesthesiology: This device is to be used by properly trained personnel to deliver emergency, short term, con
Terminated
BTLNone listed

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