CRITHIDIA LUCILLIAE DS DNA KIT (DIAGNOSTIC USE)— 510(k) K930987
Substantially EquivalentThe Binding Site, Ltd.
FDA 510(k) clearance K930987 for CRITHIDIA LUCILLIAE DS DNA KIT (DIAGNOSTIC USE), Substantially Equivalent on 1993-08-10. Applicant: The Binding Site, Ltd.. Device class: 2.
Clearance details
- Applicant
- The Binding Site, Ltd.
- Product code
- Code KTL
- Device class
- Class 2
- Regulation
- 21 CFR 866.5100
- Advisory panel
- Immunology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Los Angeles, CA, US
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More clearances from The Binding Site, Ltd.
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- K083289 — HUMAN BETA-2 MICROGLOBULIN KIT
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Data sourced from openFDA. This site is unofficial and independent of the FDA.