DIAMOND DIAGNOSTICS ISE SERUM STANDARDS, DIAMOND DIAGNOSTICS ISE URINE STANDARDS— 510(k) K133751
Substantially EquivalentDiamond Diagnostics, Inc.
FDA 510(k) clearance K133751 for DIAMOND DIAGNOSTICS ISE SERUM STANDARDS, DIAMOND DIAGNOSTICS ISE URINE STANDARDS, Substantially Equivalent on 2014-08-08. Applicant: Diamond Diagnostics, Inc.. Device class: 2.
Clearance details
- Applicant
- Diamond Diagnostics, Inc.
- Product code
- Code JIT
- Device class
- Class 2
- Regulation
- 21 CFR 862.1150
- Advisory panel
- Clinical Chemistry
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Holliston, MA, US
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Data sourced from openFDA. This site is unofficial and independent of the FDA.