ClearanceBrief
510(k) K030853 ยท FRG Wrap, Sterilization

STERITITE PERFORATED BASE RIGID REUSABLE STERILIZATION CONTAINER SYSTEM WITH SCF02-POLYPROPYLENE NON-WOVEN DISPOSABLE FI

ApplicantCase Medical, Inc., Ridgefield NJ, US
DecisionSubstantially Equivalent, Mar 21, 2003
ReceivedMar 18, 2003
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K030853

DateFirm and productCodeLinked 510(k)
Dec 3, 2013Advanced Sterilization Products
STERITITE Containers: STERITITE Container Kit, 1/4 size, 3" high, product code: 13902; STERITITE Mini Mid Size, 3" high, product code: 13903; STERITITE Container Kit, 1/2 size, 4" high, product code:
Terminated
FRGNone listed

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