PREMIER HSV PLUS— 510(k) K953839
Substantially EquivalentMeridian Diagnostics, Inc.
FDA 510(k) clearance K953839 for PREMIER HSV PLUS, Substantially Equivalent on 1996-05-23. Applicant: Meridian Diagnostics, Inc.. Device class: 2.
Clearance details
- Applicant
- Meridian Diagnostics, Inc.
- Product code
- Code LGC
- Device class
- Class 2
- Regulation
- 21 CFR 866.3305
- Advisory panel
- Microbiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Cincinnati, OH, US
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