ClearanceBrief
510(k) K881413 ยท GEI Electrosurgical, Cutting & Coagulation & Accessories

ELECTRO-CAUTERY SUCTION TUBE

ApplicantAlto Development Corp., Farmingdale NJ, US
DecisionSubstantially Equivalent, Apr 21, 1988
ReceivedApr 4, 1988
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K881413

DateFirm and productCodeLinked 510(k)
Jan 15, 2014Teleflex Medical
Weck, Electrosurgical Coagulation Suction Tube 6 (15.2cm), 11 French, with Stylet, Teleflex Medical, Research Triangle, NC 2770. Intended to remove tissue and control bleeding by use of high-frequenc
Terminated
GEINone listed
Jan 15, 2014Teleflex Medical
Weck, Electrosurgical Coagulation Suction Tube 8 (20.0cm), 11 French, with Stylet, Teleflex Medical, Research Triangle, NC 27709. Intended to remove tissue and control bleeding by use of high-frequen
Terminated
GEINone listed

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