Gesco Intl., Inc.
FDA 510(k) medical device clearances.
Top product codes for Gesco Intl., Inc.
Recent clearances by Gesco Intl., Inc.
- K954422 — PER-Q-CATH MID-LINE
- K940870 — UMBILI-CATH
- K940953 — UMBILI-CATH-S
- K940952 — UMBILI-CATH-S-DL
- K941672 — URI-CATH CATHETER
- K941232 — THORA-CATH
- K940871 — UMBILI-CATH-P
- K931989 — VENTRI-CATH
- K926063 — PER-Q-CATH DRESSING CHANGE TRAY
- K923591 — PALA-NATE
- K915167 — GESCO PER-Q-CATH CATHETER INTRODUCER
- K911326 — OBSTETRICAL VACUUM CUP
- K910652 — SPINAL TAP NEEDLE
- K911607 — GESCO UMBILI-CATH
- K911215 — GESCO PER-Q-CATH NEEDLE
- K910622 — GESCO PER-Q-CATH REPAIR KIT
- K895942 — GESCO DUAL LUMEN PER-Q-CATH-DL
- K896041 — GESCO DUAL LUMEN UMBILICATH II-DL
- K882647 — GESCO CATHETERIZATION TRAY
- K872221 — DIALY-NATE SET & DIALY-NATE CATHETER
- K870962 — GESCO ASPIRATOR
- K861090 — NUTRI-CATH - FEEDING TUBE
- K852490 — URI-CATH SYSTEM
- K851385 — THORA-CATH TROCAR-TYPE CHEST DRAINAGE TUBE
- K831845 — PER-Q-CATH TRAY
- K772288 — CATHETER, CHOLANGIOGRAM, OPERATIVE
Data sourced from openFDA. This site is unofficial and independent of the FDA.