Sil-Med Corp.
Sil-Med Corp. holds FDA 510(k) medical device clearances, first cleared 1980, most recent 1997.
Top product codes for Sil-Med Corp.
Recent clearances by Sil-Med Corp.
- K972521 — NAVIGATOR (STYLET) 2006
- K961392 — ANTIMICROBIAL PERITONEAL DIALYSIS COIL CATHETER WITH SPI-ARGENT II
- K961194 — ANTIMICROBIAL MEDIASTINAL SILICONE DRAIN
- K961295 — SAPPHIRE LINE FLAT DRAIN/KIT WITH SPI-ARGENT II W/OR W/OUT TROCAR
- K960099 — PENROSE DRAIN MODELS 6001 - 6007
- K955463 — GRIP-A-BOOTS
- K942709 — MEDIASTINAL SILICONE DRAINS
- K926496 — SIL-SLIP (COATED/REGULAR(NON-COATED)THORACIC DRAIN
- K926408 — SIL-SLIP FLAT SUCTION DRAIN
- K926495 — SIL-SLIP ROUND WOUND DRAIN (COATED)/BLUE STRIPE
- K921424 — SIL-MED FLAT SUCTION DRAIN
- K903989 — SIL-MED T-TUBE DRAIN
- K891471 — SIL-MED WASTE FLUID DUMP BAG
- K885167 — TRUDELL BENT CATHETER
- K862767 — SILICONE SUMP DRAIN
- K854418 — ROUND SUCTION DRAIN
- K851195 — VASCULAR ACCESS CATHETER
- K851196 — INCISION DRAIN
- K851921 — Y CONNECTOR
- K850247 — PERITONEAL DIALYSIS COIL CATHETER
- K843575 — DERBYSHIRE DRAIN
- K842765 — SILIMED BREAST FORM
- K833872 — SAV-A-LIMB
- K830607 — SUCTION RESERVOIR
- K830610 — FLAT SUCTION DRAIN
- K813063 — FLAT DRAIN
- K813062 — VASCULAR PAWS
- K810080 — VASCULAR TIE (VAS-TIE)
- K801818 — TENCKHOFF CATHETER
Data sourced from openFDA. This site is unofficial and independent of the FDA.