JAS URIC ACID LIQUID REAGENT— 510(k) K012038
Substantially EquivalentJas Diagnostics, Inc.
FDA 510(k) clearance K012038 for JAS URIC ACID LIQUID REAGENT, Substantially Equivalent on 2001-08-21. Applicant: Jas Diagnostics, Inc.. Device class: 1.
Clearance details
- Applicant
- Jas Diagnostics, Inc.
- Product code
- Code KNK
- Device class
- Class 1
- Regulation
- 21 CFR 862.1775
- Advisory panel
- Clinical Chemistry
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Miami, FL, US
Recent devices under product code KNK
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- K080618 — DIRECT HBA1C, FRUCTOSAMINE, GLUCOSE OXIDASE LIQUID
- K022519 — LDL CHOLESTEROL (AUTOMATED)
- K021671 — JAS HDL CHOLESTEROL (AUTOMATED) REAGENT
Data sourced from openFDA. This site is unofficial and independent of the FDA.