Quest Medical, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Quest Medical, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Lyka® PORT Needle Free Access Device (4170Y), Q2 Blood Administration Sets, Q2 IV Administration Sets
39
Total
39
Cleared
0
Denied
Quest Medical, Inc. has 39 FDA 510(k) cleared medical devices. Based in Walker, US.
Latest FDA clearance: Dec 2024. Active since 1980. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Quest Medical, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Experien Group as regulatory consultant.
FDA 510(k) Regulatory Record - Quest Medical, Inc.
39 devices
Cleared
Dec 18, 2024
Lyka® PORT Needle Free Access Device (4170Y)
General Hospital
244d
Cleared
Jun 05, 2022
Q2 Blood Administration Sets
General Hospital
177d
Cleared
Jun 02, 2022
Q2 IV Administration Sets
General Hospital
202d
Cleared
Jan 21, 2021
Precision Delivery Infusion Set
General Hospital
128d
Cleared
Nov 20, 2020
MPS 3 ND Myocardial Protection System
Cardiovascular
126d
Cleared
Jun 19, 2020
MPS 3 Myocardial Protection System
Cardiovascular
116d
Cleared
Nov 06, 2018
MiniGuard Arterial Safety Valve
Cardiovascular
60d
Cleared
Oct 01, 2018
MPS2 Myocardial Protection System Console
Cardiovascular
300d
Cleared
Mar 08, 2017
Q2 Low Pressure Power Injection Extension Set
General Hospital
154d
Cleared
Dec 06, 2016
Q2 Multiport IV Administration Sets and Extension Sets, Checkmate Multiport...
General Hospital
111d
Cleared
Sep 30, 2015
Q2 Intravenous Adminstration Sets and Extension Sets
General Hospital
161d
Cleared
Oct 19, 2012
LACRICATH LACRIMAL DUCT CATHETER
Ophthalmic
294d
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