AIM-V (R) MEDIUM, MODEL 087-0112— 510(k) K022086
Substantially EquivalentInvitrogen Corporation
FDA 510(k) clearance K022086 for AIM-V (R) MEDIUM, MODEL 087-0112, Substantially Equivalent on 2002-12-23. Applicant: Invitrogen Corporation.
Clearance details
- Applicant
- Invitrogen Corporation
- Product code
- Code NDS
- Advisory panel
- Gastroenterology, Urology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Grand Island, NY, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.