ROTAVIRUS ENZYME IMMUNOASSAY— 510(k) K843367
Substantially EquivalentIntl. Diagnostic Laboratories, Ltd.
FDA 510(k) clearance K843367 for ROTAVIRUS ENZYME IMMUNOASSAY, Substantially Equivalent on 1985-06-13. Applicant: Intl. Diagnostic Laboratories, Ltd..
Clearance details
- Applicant
- Intl. Diagnostic Laboratories, Ltd.
- Product code
- Code LIQ
- Advisory panel
- Microbiology
- 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.