ClearanceBrief
510(k) K983519 ยท KMF Bandage, Liquid

COMFEEL SEASORB DRESSING

ApplicantColoplast Corp., Marietta GA, US
DecisionSubstantially Equivalent, Dec 30, 1998
ReceivedOct 8, 1998
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K983519

DateFirm and productCodeLinked 510(k)
Apr 4, 2007Coloplast Corp Skin Care Div
Sea-Clens Wound Cleanser, 6 fl. oz., Manufactured by Coloplast Corp., Marietta, GA, #11701-159-36, #1063.
Terminated
KMFNone listed

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