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FDA 510(k) Applications Submitted by Kay Fuller
FDA 510(k) Number
Submission Date
Device Name
Applicant
K120839
03/20/2012
NOVACATH SECURE IV CATHETER SYSTEM-18G
TANGENT MEDICAL TECHNOLOGIES, INC.
K210843
03/22/2021
STAGE
SpinTech, Inc.
K022236
07/11/2002
RECOVERY FILTER SYSTEM, MODEL RF-048F
C.R. BARD, INC.
K173224
10/03/2017
SPIN-SWI
SpinTech, Inc.
K173725
12/05/2017
NeuMoDx GBS Assay
NeuMoDx Molecular, Inc.
K090341
02/10/2009
MICHIGAN CRANIAL RESHAPING ORTHOSIS
DANMAR PRODUCTS, INC.
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