R&D HGB/GLC WHOLE BLOOD CONTROL— 510(k) K993321
Substantially EquivalentR&D Systems, Inc.
FDA 510(k) clearance K993321 for R&D HGB/GLC WHOLE BLOOD CONTROL, Substantially Equivalent on 1999-11-12. Applicant: R&D Systems, Inc..
Clearance details
- Applicant
- R&D Systems, Inc.
- Product code
- Code GGM
- Advisory panel
- Hematology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Minneapolis, MN, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.