ClearanceBrief
510(k) K812648 ยท KNT Tubes, Gastrointestinal (And Accessories)

EHTOX GASTRIC LAVAGE KIT #2050 & #2070

ApplicantEthox Corp., Mchenry IL, US
DecisionSubstantially Equivalent, Sep 29, 1981
ReceivedSep 17, 1981
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K812648

DateFirm and productCodeLinked 510(k)
Nov 22, 2011Ethox International, Inc.
TUM-E-VAC REF 2075, Rx ONLY, NON STERILE --- Ethox International, Buffalo, NY 14204, USA --- Intended use: gastric lavage
Terminated
KNTNone listed

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