Latex Ind., Inc.
Latex Ind., Inc. holds FDA 510(k) medical device clearances, first cleared 1977, most recent 1981.
Top product codes for Latex Ind., Inc.
Recent clearances by Latex Ind., Inc.
- K812058 — AKRON URINARY DRAINAGE BAT
- K810281 — UROLOGICAL CATHETERS
- K791674 — BLADDER RETENTION CATHETERIZATION TRAY
- K781751 — CATHETER, AKRON FOLEY TEFLON
- K781433 — AKRON MALE EXTERNAL CATHETER
- K772277 — BLADDER RETENTION-CATHETHERIZATIONTRAY
- K772340 — CATHETERIZATION KIT 732016-732018
- K772341 — BLADDER KIT - 734000
- K772342 — ROBINSON KIT - 750014 & 750016
- K780267 — CATH TRAY W/OUT CATHETER
- K780268 — BLADDER CATH KIT W/OUT CATHETER
- K771650 — AKRO-SIL FOLEY KIT 30CC
- K771651 — AKRO-SIL FOLEY KIT 5CC
- K771652 — CATH-CARE TRAY
Data sourced from openFDA. This site is unofficial and independent of the FDA.