DRX NTX OR, OSTEOMARK NTX DIRECT RESPONSE— 510(k) K984530
Substantially EquivalentMetrika, Inc.
FDA 510(k) clearance K984530 for DRX NTX OR, OSTEOMARK NTX DIRECT RESPONSE, Substantially Equivalent on 1999-08-10. Applicant: Metrika, Inc.. Device class: 2.
Clearance details
- Applicant
- Metrika, Inc.
- Product code
- Code JFY
- Device class
- Class 2
- Regulation
- 21 CFR 862.1225
- Advisory panel
- Clinical Chemistry
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Los Angeles, CA, US
Recent devices under product code JFY
view allMore clearances from Metrika, Inc.
view allData sourced from openFDA. This site is unofficial and independent of the FDA.