INFLUENZA A ANTIGEN TEST— 510(k) K942172
Substantially EquivalentNeogenex
FDA 510(k) clearance K942172 for INFLUENZA A ANTIGEN TEST, Substantially Equivalent on 1994-07-06. Applicant: Neogenex. Device class: 1.
Clearance details
- Applicant
- Neogenex
- Product code
- Code GNW
- Device class
- Class 1
- Regulation
- 21 CFR 866.3330
- Advisory panel
- Microbiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Everett, WA, US
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More clearances from Neogenex
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