Gesco Intl., Inc.
Gesco Intl., Inc. holds FDA 510(k) medical device clearances, first cleared 1978, most recent 1995.
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.