HEPARIN CONTROL KIT— 510(k) K943520
UnknownAmerican Bioproducts Co.
FDA 510(k) clearance K943520 for HEPARIN CONTROL KIT, Unknown on 1995-09-26. Applicant: American Bioproducts Co.. Device class: 2.
Clearance details
- Applicant
- American Bioproducts Co.
- Product code
- Product code KFF
- Device class
- Class 2
- Regulation
- 21 CFR 864.7525
- Advisory panel
- Hematology
- Date received
- Decision date
- Decision
- Unknown
- Clearance type
- Traditional
- Location
- Parisppany, NJ, US
Recent devices under product code KFF
view all- K260214 — STA® - Liquid Anti-Xa
- K213464 — HemosIL Liquid Anti-Xa
- K162540 — INNOVANCE(r) Heparin Reagents, INNOVANCE(r) Heparin Calibrator, INNOVANCE(r) Heparin UF and Heparin LMW Controls
- K111822 — STA(R) - LIQUID ANTI-XA, MULTI HEP CALIBRATOR, QUALITY HNF / UFH, QUALITY HBPM / LMWH
- K090209 — HEMOSIL LIQUID HEPARIN, HEPARIN CALIBRATORS AND LMW AND UF HEPARIN CONTROLS
More clearances from American Bioproducts Co.
view allData sourced from openFDA. This site is unofficial and independent of the FDA.