ARTIMICROBIAL REMOVAL DEVICE— 510(k) K830372
Substantially EquivalentMarion Laboratories, Inc.
FDA 510(k) clearance K830372 for ARTIMICROBIAL REMOVAL DEVICE, Substantially Equivalent on 1983-04-08. Applicant: Marion Laboratories, Inc.. Device class: 1.
Clearance details
- Applicant
- Marion Laboratories, Inc.
- Product code
- Code LJF
- Device class
- Class 1
- Regulation
- 21 CFR 866.2560
- Advisory panel
- Microbiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Walker, MI, US
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