Cair Lgl is one of 16115 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Cair Lgl - FDA 510(k) Cleared Devices
Recent clearances: Nutricair enteral ENFit adapter: ENFit male – stepped/Christmas tree connector, Nutricair Enteral Syringe with ENFit, Nasogastric Feeding Tubes - ENFit Port - PVC
8
Total
8
Cleared
0
Denied
Cair Lgl has 8 FDA 510(k) cleared medical devices. Based in New York, US.
Latest FDA clearance: Jan 2024. Active since 2014. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Cair Lgl Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Vesco Medical and Wiesen Law Offices.
FDA 510(k) Regulatory Record - Cair Lgl
8 devices
Cleared
Jan 22, 2024
Nutricair enteral ENFit adapter: ENFit male – stepped/Christmas tree connector
Gastroenterology & Urology
263d
Cleared
Oct 06, 2023
Nutricair Enteral Syringe with ENFit
Gastroenterology & Urology
155d
Cleared
Jun 09, 2022
Nasogastric Feeding Tubes - ENFit Port - PVC
Gastroenterology & Urology
252d
Cleared
Nov 02, 2021
Pediatric Nasogastric Feeding Tubes - Single ENFit Port
Gastroenterology & Urology
246d
Cleared
Sep 01, 2017
Carefusion NeutraClear Needle-free connector (EL-NC1000)
General Hospital
140d
Cleared
Aug 15, 2017
Carefusion NeutraClear multi-fuse Extension Set with needle-free connector(s)
General Hospital
123d
Cleared
Jul 31, 2017
Carefusion NeutraClear Needle-free connector
General Hospital
105d
Cleared
Mar 20, 2014
CAIR DRIVE, NEUTRACLEAR
General Hospital
171d