ClearanceBrief
510(k) K121607 ยท FMI Needle, Hypodermic, Single Lumen

TERUMO(R) NEEDLE

ApplicantTerumo (Philippines) Corporation, Elkton MD, US
DecisionSubstantially Equivalent, Nov 8, 2012
ReceivedJun 1, 2012
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K121607

DateFirm and productCodeLinked 510(k)
Feb 8, 2019Terumo Medical Corporation
Terumo Sur-vet Needle, 20G x 1", Product Code 100204
Terminated
FMINone listed
Feb 8, 2019Terumo Medical Corporation
Terumo Sur-vet Needle, 22G x 1", Product Code 100211
Terminated
FMINone listed
Feb 8, 2019Terumo Medical Corporation
Terumo Sur-vet Needle, 22G x 3/4", Product Code 100215
Terminated
FMINone listed
Feb 8, 2019Terumo Medical Corporation
Terumo Sur-vet Needle, 25G x 5/8", Product Code 100220
Terminated
FMINone listed
Feb 8, 2019Terumo Medical Corporation
Terumo Sur-vet Needle, 22G x 3/4", Product Code 100279
Terminated
FMINone listed
Feb 8, 2019Terumo Medical Corporation
Terumo Sur-vet Needle, 25G x 5/8", Product Code 100280
Terminated
FMINone listed
Feb 8, 2019Terumo Medical Corporation
Terumo Needle, 18G x 1", Product Code NN1825R
Terminated
FMINone listed
Feb 8, 2019Terumo Medical Corporation
Terumo Needle, 23G x 1", Product Code NN2325R
Terminated
FMINone listed
Feb 8, 2019Terumo Medical Corporation
Terumo Needle, 30G x 1/2", Product Code NN3013R
Terminated
FMINone listed

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