Diasol, Inc.
Diasol, Inc. holds FDA 510(k) medical device clearances, first cleared 1999, most recent 2014, with 8 FDA device recalls on record.
Top product codes for Diasol, Inc.
FDA recalls by Diasol, Inc.
- Z-0989-2026 — Brand Name: Diasol Product Name: 100220-10-DEX100, Liquid Concentrate for Bicarbonate Dialysis Non Pyrogenic, 2K, 3.0CA, 1.0MG, 208.2 liters
- Z-0991-2026 — Brand Name: Diasol Product Name: 100325-10-DEX100, Liquid Concentrate for Bicarbonate Dialysis Non Pyrogenic, 2K, 3.0CA, 1.0MG, 208.2 liters
- Z-0992-2026 — Brand Name: Diasol Product Name: 100425-10-DEX100, Liquid Concentrate for Bicarbonate Dialysis Non Pyrogenic, 2K, 3.0CA, 1.0MG, 208.2 liters
- Z-0990-2026 — Brand Name: Diasol Product Name: 100230-10-DEX100, Liquid Concentrate for Bicarbonate Dialysis Non Pyrogenic, 2K, 3.0CA, 1.0MG, 208.2 liters
- Z-0987-2026 — Brand Name: Diasol Product Name: 100225-10-DEX100, Liquid Concentrate for Bicarbonate Dialysis Non Pyrogenic, 2K, 3.0CA, 1.0MG, 208.2 liters
- Z-0988-2026 — Brand Name: Diasol Product Name: 100125-10-DEX100, Liquid Concentrate for Bicarbonate Dialysis Non Pyrogenic, 2K, 3.0CA, 1.0MG, 208.2 liters
- Z-0207-2025 — Diasol Acid Concentrate REF G100325-10Dex 100
- Z-2402-2020 — DIASOL 1000225-10-DEX100 LIQUID ACID CONCENTRATE FOR BICARBONATE DIALYSIS
Recalls are matched by FDA's recalling-firm name — openFDA's enforcement dataset doesn't reference 510(k) numbers, so a recall here may cover devices beyond this company's 510(k) clearances.
Recent clearances by Diasol, Inc.
- K130511 — CITRISOL ACID CONCENTRATE
- K020231 — DIASOL-ADDITIVES
- K020230 — DIASOL-BICARB
- K011004 — NEEDLELOK HYPODERMIC NEEDLE PROTECTION
- K010958 — FISTULOK FISTULA NEEDLE PROTECTION
- K011003 — SAFESTING AND SAFESTING HUB
- K992999 — DAISY PROTECTED SCALP VEIN SET
- K993187 — SHELLY PROTECTED AV FISTULA NEEDLE
- K992653 — SHELLY PROTECTED AV FISTULA NEEDLE
- K993212 — DRYASOL ACID CONCENTRATE MIX
Data sourced from openFDA. This site is unofficial and independent of the FDA.