INTERLINK THREADED LOCK CANNULA

Set, Administration, Intravascular

BD

The following data is part of a premarket notification filed by Bd with the FDA for Interlink Threaded Lock Cannula.

Pre-market Notification Details

Device IDK011858
510k NumberK011858
Device Name:INTERLINK THREADED LOCK CANNULA
ClassificationSet, Administration, Intravascular
Applicant BD 1 BECTON DR. MC 226 Franklin Lakes,  NJ  07417
ContactGregory W Morgan
CorrespondentGregory W Morgan
BD 1 BECTON DR. MC 226 Franklin Lakes,  NJ  07417
Product CodeFPA  
CFR Regulation Number880.5440 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeSpecial
3rd Party ReviewedNo
Combination ProductNo
Date Received2001-06-14
Decision Date2001-06-19
Summary:summary

NIH GUDID Devices

Device IdentifiersubmissionNumberSupplement
50382903033695 K011858 000
30382903033790 K011858 000

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