PARA-PAK PLUS— 510(k) K931770
Substantially EquivalentMeridian Diagnostics, Inc.
FDA 510(k) clearance K931770 for PARA-PAK PLUS, Substantially Equivalent on 1993-06-15. Applicant: Meridian Diagnostics, Inc.. Device class: 1.
Clearance details
- Applicant
- Meridian Diagnostics, Inc.
- Product code
- Code LIO
- Device class
- Class 1
- Regulation
- 21 CFR 866.2900
- Advisory panel
- Microbiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Cincinnati, OH, US
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