MDI SM TEST— 510(k) K994029
Substantially EquivalentMicro Detect, Inc.
FDA 510(k) clearance K994029 for MDI SM TEST, Substantially Equivalent on 2000-01-11. Applicant: Micro Detect, Inc.. Device class: 2.
Clearance details
- Applicant
- Micro Detect, Inc.
- Product code
- Code LLL
- Device class
- Class 2
- Regulation
- 21 CFR 866.5100
- Advisory panel
- Immunology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Tustin, CA, US
Recent devices under product code LLL
view allMore clearances from Micro Detect, Inc.
view allData sourced from openFDA. This site is unofficial and independent of the FDA.