ClearanceBrief
510(k) K811234 ยท KPE Container, I.V.

I.V. BOTTLE (RIDGID)

ApplicantMedi-Plast Intl., Inc., Walker MI, US
DecisionSubstantially Equivalent, Jun 18, 1981
ReceivedMay 4, 1981
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K811234

DateFirm and productCodeLinked 510(k)
Aug 16, 2024Microtek Medical Inc.
Bottle Decanter, REF 2004S. Packaged on a form, fill and seal machine with a poly/Tyvek material then placed 50 products to a case (cs).
Open, Classified
KPENone listed

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