LITHIUM INTERNAL STANDARD 3000 MEQ/L #60084— 510(k) K871187
Substantially EquivalentIn Vitro Diagnostics, Inc.
FDA 510(k) clearance K871187 for LITHIUM INTERNAL STANDARD 3000 MEQ/L #60084, Substantially Equivalent on 1987-05-28. Applicant: In Vitro Diagnostics, Inc.. Device class: 2.
Clearance details
- Applicant
- In Vitro Diagnostics, Inc.
- Product code
- Code JIS
- Device class
- Class 2
- Regulation
- 21 CFR 862.1150
- Advisory panel
- Clinical Chemistry
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Shelton, CT, US
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