LANCER MSA BUN DIAG. KIT— 510(k) K821562
Substantially EquivalentSherwood Medical Co.
FDA 510(k) clearance K821562 for LANCER MSA BUN DIAG. KIT, Substantially Equivalent on 1982-06-11. Applicant: Sherwood Medical Co.. Device class: 2.
Clearance details
- Applicant
- Sherwood Medical Co.
- Product code
- Code CDQ
- Device class
- Class 2
- Regulation
- 21 CFR 862.1770
- Advisory panel
- Clinical Chemistry
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Walker, MI, US
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Data sourced from openFDA. This site is unofficial and independent of the FDA.