ANTIMICROBIAL REMOVAL DEVICE (ARD)— 510(k) K800052
Substantially EquivalentMarion Laboratories, Inc.
FDA 510(k) clearance K800052 for ANTIMICROBIAL REMOVAL DEVICE (ARD), Substantially Equivalent on 1980-04-04. Applicant: Marion Laboratories, Inc..
Clearance details
- Applicant
- Marion Laboratories, Inc.
- Advisory panel
- Unknown
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Mchenry, IL, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.